Requirement of macrophages and eosinophils and their cytokines/chemokines for mammary gland development

The TNF and TNF Receptor Superfamilies

Locksley, R. M., Killeen, N., & Lenardo, M. J. (2001) · Cell · doi:10.1016/s0092-8674(01)00237-9 · Cited by 3,650 · see citing works

Secretory products of macrophages.

Nathan, C. F. (1987) · Journal of Clinical Investigation · doi:10.1172/jci112815 · Cited by 2,615 · see citing works

Human Chemokines: An Update

Baggiolini, M., Dewald, B., & Moser, B. (1997) · Annual Review of Immunology · doi:10.1146/annurev.immunol.15.1.675 · Cited by 2,193 · see citing works

The role of tumour‐associated macrophages in tumour progression: implications for new anticancer therapies

Bingle, L., Brown, N. J., & Lewis, C. E. (2002) · The Journal of Pathology · doi:10.1002/path.1027 · Cited by 2,022 · see citing works

The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene

Yoshida, H., Hayashi, S.-I., Kunisada, T., Ogawa, M., Nishikawa, S., Okamura, H., Sudo, T., Shultz, L. D., & Nishikawa, S.-I. (1990) · Nature · doi:10.1038/345442a0 · Cited by 1,789 · see citing works

Colony-Stimulating Factor 1 Promotes Progression of Mammary Tumors to Malignancy

Lin, E. Y., Nguyen, A. V., Russell, R. G., & Pollard, J. W. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.193.6.727 · Cited by 1,594 · see citing works

The c-fms proto-oncogene product is related to the receptor for the mononuclear phagocyte growth factor, CSF 1

Sherr, C. J., Rettenmier, C. W., Sacca, R. E., Roussel, M. F., Look, A. T., & Stanley, E. R. (1985) · Cell · doi:10.1016/s0092-8674(85)80047-7 · Cited by 1,539 · see citing works

Association of macrophage infiltration with angiogenesis and prognosis in invasive breast carcinoma.

Leek, R., Lewis, C. E., Whitehouse, R. M., Greenall, M. J., Clarke, J., & Harris, A. L. (1996) · PubMed · Cited by 1,187 · see citing works

Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects

Dai, X.-M., Ryan, G. R., Hapel, A. J., Dominguez, M. G., Russell, R. G., Kapp, S., Sylvestre, V., & Stanley, E. R. (2002) · Blood · doi:10.1182/blood.v99.1.111 · Cited by 1,184 · see citing works

The origin and function of tumor-associated macrophages

Mantovani, A., Bottazzi, B., Colotta, F., Sozzani, S., & Ruco, L. P. (1992) · Immunology Today · doi:10.1016/0167-5699(92)90008-u · Cited by 1,088 · see citing works

Selective Expression of the Eotaxin Receptor CCR3 by Human T Helper 2 Cells

Sallusto, F., Mackay, C. R., & Lanzavecchia, A. (1997) · Science · doi:10.1126/science.277.5334.2005 · Cited by 1,050 · see citing works

Total absence of colony-stimulating factor 1 in the macrophage-deficient osteopetrotic (op/op) mouse.

Wiktor-Jedrzejczak, W., Bartocci, A., Ferrante, A. W., Ahmed-Ansari, A., Sell, K. W., Pollard, J. W., & Stanley, E. R. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4828 · Cited by 1,031 · see citing works

Interleukin-5, eosinophils, and disease

Sanderson, C. (1992) · Blood · doi:10.1182/blood.v79.12.3101.bloodjournal79123101 · Cited by 972 · see citing works

Interleukin-5, eosinophils, and disease

Sanderson, C. (1992) · Blood · doi:10.1182/blood.v79.12.3101.3101 · Cited by 860 · see citing works

Eosinophilia

Rothenberg, M. E. (1998) · New England Journal of Medicine · doi:10.1056/nejm199805283382206 · Cited by 837 · see citing works

The Eosinophilic Leukocyte: Structure and Function

Gleich, G. J., & Adolphson, C. R. (1986) · Advances in immunology · doi:10.1016/s0065-2776(08)60351-x · Cited by 822 · see citing works

RANK-L and RANK: T Cells, Bone Loss, and Mammalian Evolution

Theill, L. E., Boyle, W. J., & Penninger, J. M. (2002) · Annual Review of Immunology · doi:10.1146/annurev.immunol.20.100301.064753 · Cited by 817 · see citing works

The osteoclast differentiation factor osteoprotegerin ligand is essential for mammary gland development.

Fata, J. E., Kong, Y.-Y., Li, J., Sasaki, T., Irie-Sasaki, J., Moorehead, R. A., Elliott, R., Scully, S., Voura, E. B., Lacey, D. L., et al. (2000) · Cell · doi:10.1016/s0092-8674(00)00103-3 · Cited by 756 · see citing works

Human eotaxin is a specific chemoattractant for eosinophil cells and provides a new mechanism to explain tissue eosinophilia

García-Zepeda, E. A., Rothenberg, M. E., Ownbey, R. T., Celestin, J., Leder, P., & Luster, A. D. (1996) · Nature Medicine · doi:10.1038/nm0496-449 · Cited by 683 · see citing works

Survival of mononuclear phagocytes depends on a lineage-specific growth factor that the differentiated cells selectively destroy

Tushinski, R. J., Oliver, I. T., Guilbert, L. J., Tynan, P. W., Warner, J. R., & Stanley, E. R. (1982) · Cell · doi:10.1016/0092-8674(82)90376-2 · Cited by 663 · see citing works

Immunobiology of the Mammary Gland

Sordillo, L. M., Shafer-Weaver, K., & DeRosa, D. C. (1997) · Journal of Dairy Science · doi:10.3168/jds.s0022-0302(97)76121-6 · Cited by 544 · see citing works

Targeted Disruption of the Chemokine Eotaxin Partially Reduces Antigen-induced Tissue Eosinophilia

Rothenberg, M. E., MacLean, J. A., Pearlman, E. M., Luster, A. D., & Leder, P. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.4.785 · Cited by 524 · see citing works

CSF‐1—A mononuclear phagocyte lineage‐specific hemopoietic growth factor

Stanley, E. R., Guilbert, L. J., Tushinski, R. J., & Bartelmez, S. H. (1983) · Journal of Cellular Biochemistry · doi:10.1002/jcb.240210206 · Cited by 516 · see citing works

High expression of the chemokine receptor CCR3 in human blood basophils. Role in activation by eotaxin, MCP-4, and other chemokines.

Uguccioni, M., Mackay, C. R., Ochensberger, B., Loetscher, P., Rhis, S., LaRosa, G. J., Rao, P. E., Ponath, P. D., Baggiolini, M., & Dahinden, C. A. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119624 · Cited by 482 · see citing works

Postnatal mammary gland development requires macrophages and eosinophils

Gouon–Evans, V., Rothenberg, M. E., & Pollard, J. W. (2000) · Development · doi:10.1242/dev.127.11.2269 · Cited by 463 · see citing works

Tumor-induced immune dysfunction: the macrophage connection

Elgert, K. D., Alleva, D. G., & Mullins, D. W. (1998) · Journal of Leukocyte Biology · doi:10.1002/jlb.64.3.275 · Cited by 426 · see citing works

Microenvironmental influence on macrophage regulation of angiogenesis in wounds and malignant tumors

Crowther, M., Brown, N. J., Bishop, E., & Lewis, C. E. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.70.4.478 · Cited by 414 · see citing works

Fundamental signals that regulate eosinophil homing to the gastrointestinal tract

Mishra, A., Hogan, S. P., Lee, J. J., Foster, P. S., & Rothenberg, M. E. (1999) · Journal of Clinical Investigation · doi:10.1172/jci6560 · Cited by 399 · see citing works

Origin of IgA-secreting plasma cells in the mammary gland.

Roux, M. E., McWilliams, M., Phillips‐Quagliata, J. M., Weisz-Carrington, P., & Lamm, M. E. (1977) · The Journal of Experimental Medicine · doi:10.1084/jem.146.5.1311 · Cited by 381 · see citing works

Tumor-Associated Macrophages in Breast Cancer

Leek, R., & Harris, A. L. (2002) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/a:1020304003704 · Cited by 353 · see citing works

Murine eotaxin: an eosinophil chemoattractant inducible in endothelial cells and in interleukin 4-induced tumor suppression.

Rothenberg, M. E., Luster, A. D., & Leder, P. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8960 · Cited by 345 · see citing works

Eotaxin Induces a Rapid Release of Eosinophils and Their Progenitors From the Bone Marrow

Palframan, R. T., COLLINS, P. D., Williams, T. J., & Rankin, S. M. (1998) · Blood · doi:10.1182/blood.v91.7.2240 · Cited by 293 · see citing works

The Macrophage Growth Factor CSF-1 in Mammary Gland Development and Tumor Progression

Lin, E. Y., Gouon–Evans, V., Nguyen, A., & Pollard, J. W. (2002) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/a:1020399802795 · Cited by 292 · see citing works

Eotaxin is required for the baseline level of tissue eosinophils

Matthews, A. N., Friend, D. S., Zimmermann, N., Sarafi, M. N., Luster, A. D., Pearlman, E. M., Wert, S. E., & Rothenberg, M. E. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6273 · Cited by 288 · see citing works

Mouse Eotaxin Expression Parallels Eosinophil Accumulation during Lung Allergic Inflammation but It Is Not Restricted to a Th2-Type Response

Gonzalo, J.-A., Jia, G.-Q., Aguirre, V., Friend, D. S., Coyle, A. J., Jenkins, N. A., Lin, G.-S., Katz, H. R., Lichtman, A. H., Copeland, N. G., et al. (1996) · Immunity · doi:10.1016/s1074-7613(00)80293-9 · Cited by 262 · see citing works

Apoptosis in the terminal endbud of the murine mammary gland: a mechanism of ductal morphogenesis

Humphreys, R. C., Krajewska, M., Krnacik, S., Jæger, R., Weiher, H., Krajewski, S., Reed, J. C., & Rosen, J. M. (1996) · Development · doi:10.1242/dev.122.12.4013 · Cited by 260 · see citing works

Molecular Cloning of F4/80, a Murine Macrophage-restricted Cell Surface Glycoprotein with Homology to the G-protein-linked Transmembrane 7 Hormone Receptor Family

McKnight, A. J., Macfarlane, A., Dri, P., TURLEY, L., Willis, A. C., & Gordon, S. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.1.486 · Cited by 229 · see citing works

Anti-Colony-Stimulating Factor-1 Antibody Staining in Primary Breast Adenocarcinomas Correlates With Marked Inflammatory Cell Infiltrates and Prognosis

Scholl, S. M., Pallud, C., Beuvon, F., Hacene, K., Stanley, E. R., Rohrschneider, L., Tang, R., Pouillart, P., & Lidereau, R. (1994) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/86.2.120 · Cited by 226 · see citing works

Rescue of the colony-stimulating factor 1 (CSF-1)–nullizygous mouse (Csf1op/Csf1op) phenotype with a CSF-1 transgene and identification of sites of local CSF-1 synthesis

Ryan, G. R., Dai, X.-M., Dominguez, M. G., Tong, W., Chuan, F.-C., Chisholm, O., Russell, R. G., Pollard, J. W., & Stanley, E. R. (2001) · Blood · doi:10.1182/blood.v98.1.74 · Cited by 224 · see citing works

Relationship between 5-fluorouracil (5-FU) dose intensity and therapeutic response in patients with advanced colorectal cancer receiving infusional therapy containing 5-FU

Gamelin, E. C., Danquechin‐Dorval, E., Dumesnil, Y., Maillart, P., Goudier, M.-J., Burtin, P. C., Delva, R., Lortholary, A. H., Gesta, P., & Larra, F. (1996) · Cancer · doi:10.1002/(sici)1097-0142(19960201)77:3 · Cited by 217 · see citing works

The Biology of CSF-1 and Its Receptor

Roth, P., & Stanley, E. R. (1992) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-77377-8_5 · Cited by 214 · see citing works

Regulation of Mammary Gland Development by Tissue Interaction

Robinson, G. W., Karpf, A. B. C., & Kratochwil, K. (1999) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/a:1018748418447 · Cited by 186 · see citing works

Dysmyelopoietic syndromes a search for prognostic factors in 193 patients

Coiffier, B., Adeleine, P., Viala, J. J., Bryon, P. A., Fiere, D. M., Gentilhomme, O., & Vuvan, H. (2006) · Cancer · doi:10.1002/1097-0142(19830701)52:1 · Cited by 182 · see citing works

Colony stimulating factor 1 is required for mammary gland development during pregnancy.

Pollard, J. W., & Hennighausen, L. G. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.20.9312 · Cited by 180 · see citing works

Differential Regulation of Eosinophil Chemokine Signaling Via CCR3 and Non-CCR3 Pathways

Sabroe, I., Hartnell, A., Jopling, L. A., Bel, S., Ponath, P. D., Pease, J. E., COLLINS, P. D., & Williams, T. J. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.5.2946 · Cited by 173 · see citing works

Branching morphogenesis of human mammary epithelial cells in collagen gels

Berdichevsky, F., Alford, D., D’Souza, B., & Taylor‐Papadimitriou, J. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.12.3557 · Cited by 160 · see citing works

Eosinophils and human cancer.

Samoszuk, M. K. (1997) · PubMed · Cited by 156 · see citing works

Immune Surveillance of Mammary Tissue by Phagocytic Cells

Paape, M. J., Shafer-Weaver, K., Capuco, A. V., Oostveldt, K. V., & Burvenich, C. (2002) · Advances in experimental medicine and biology · doi:10.1007/0-306-46832-8_31 · Cited by 155 · see citing works

Cells and Cytokines in Inflammatory Secretions of Bovine Mammary Gland

Riollet, C., Rainard, P., & Poutrel, B. (2005) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-46832-8_30 · Cited by 147 · see citing works

Role of dimerization and modification of the CSF‐1 receptor in its activation and internalization during the CSF‐1 response.

Li, W., & Stanley, E. R. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07948.x · Cited by 146 · see citing works

Malignant tumor and eosinophils: I. Prognostic significance in gastric cancer

Iwasaki, K., Torisu, M., & Fujimura, T. (1986) · Cancer · doi:10.1002/1097-0142(19860915)58:6 · Cited by 134 · see citing works

HIN-1, a putative cytokine highly expressed in normal but not cancerous mammary epithelial cells

Krop, I. E., Sgroi, D. C., PORTER, D. A., Lunetta, K. L., LeVangie, R., Seth, P., Kaelin, C. M., Rhei, E., Bosenberg, M., Schnitt, S. J., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.171138398 · Cited by 130 · see citing works

Colony Stimulating Factor-1 Is Required to Recruit Macrophages into the Mammary Gland to Facilitate Mammary Ductal Outgrowth

Nguyen, A., & Pollard, J. W. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0669 · Cited by 125 · see citing works

FMS (CSF-1 receptor) and CSF-1 transcripts and protein are expressed by human breast carcinomas in vivo and in vitro.

Bm, K., Ka, S., Carter, D., Ld, Y., Sapi, E., King, B. L., Chambers, S., Jones, M. A., Pirro, M. H., & Er, S. (1991) · PubMed · Cited by 121 · see citing works

Tumour‐associated leucocytes: Friends or foes in breast carcinoma

O'Sullivan, C., & Lewis, C. E. (1994) · The Journal of Pathology · doi:10.1002/path.1711720302 · Cited by 119 · see citing works

Dual origin of mesenchymal tissues participating in mouse mammary gland embryogenesis

Sakakura, T., Sakagami, Y., & Nishizuka, Y. (1982) · Developmental Biology · doi:10.1016/0012-1606(82)90024-0 · Cited by 116 · see citing works

Prognostic significance of eosinophils and mast cells in rectal cancer: Findings from the National Surgical Adjuvant Breast and Bowel Project (protocol R-01)

Fisher, E. R., Paik, S., Rockette, H. E., Jones, J., Caplan, R. J., & Fisher, B. (1989) · Human Pathology · doi:10.1016/0046-8177(89)90180-9 · Cited by 115 · see citing works

Cytokines, Chemokines, and Colony-Stimulating Factors in Human Milk: The 1997 Update

Garofalo, R. P., & Goldman, A. S. (1998) · Neonatology · doi:10.1159/000014019 · Cited by 113 · see citing works

Eotaxin Is Required for Eosinophil Homing into the Stroma of the Pubertal and Cycling Uterus

Gouon–Evans, V., & Pollard, J. W. (2001) · Endocrinology · doi:10.1210/endo.142.10.8459 · Cited by 112 · see citing works

Immune Components in Porcine Mammary Secretions

Wagstrom, E. A., Yoon, K. J., & Zimmerman, J. J. (2000) · Viral Immunology · doi:10.1089/08828240050144699 · Cited by 112 · see citing works

Cytokines in human milk: Properties and potential effects upon the mammary gland and the neonate

Goldman, A. S., Chheda, S., Garofalo, R. P., & Schmalstieg, F. C. (1996) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/bf02018078 · Cited by 110 · see citing works

Pleiotropic Roles for CSF-1 in Development Defined by the Mouse Mutation Osteopetrotic

Pollard, J. W., & Stanley, E. R. (1996) · Advances in developmental biochemistry · doi:10.1016/s1064-2722(08)60060-2 · Cited by 105 · see citing works

Eotaxin Is a Potent Chemotaxin for Human Basophils

Yamada, H., Hirai, K., Miyamasu, M., Iikura, M., Misaki, Y., Shoji, S., Takaishi, T., Kasahara, T., Morita, Y., & Ito, K. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6100 · Cited by 102 · see citing works

The regulation of macrophage protein turnover by a colony stimulating factor (CSF‐1)

Tushinski, R. J., & Stanley, E. R. (1983) · Journal of Cellular Physiology · doi:10.1002/jcp.1041160111 · Cited by 97 · see citing works

The Importance of the Eosinophil in Head and Neck Cancer

Goldsmith, M. M., Belchis, D., Cresson, D. H., Merritt, W. D., & Askin, F. B. (1992) · Otolaryngology · doi:10.1177/019459989210600124 · Cited by 95 · see citing works

HCC-2, a human chemokine: Gene structure, expression pattern, and biological activity

Pardigol, A., Forssmann, U., Zucht, H., Loetscher, P., Schulz‐Knappe, P., Baggiolini, M., Forssmann, W., & Mägert, H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.11.6308 · Cited by 95 · see citing works

Normal breast epithelial cells produce interleukins 6 and 8 together with tumor‐necrosis factor: Defective il6 expression in mammary carcinoma

Basolo, F., Conaldi, P. G., Fiore, L., Calvo, S., & Toniolo, A. (1993) · International Journal of Cancer · doi:10.1002/ijc.2910550609 · Cited by 92 · see citing works

Role of the macrophage in angiogenesis-dependent diseases

Polverini, P. J. (1997) · Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions · doi:10.1007/978-3-0348-9006-9_2 · Cited by 88 · see citing works

Production of interleukin-6 and interleukin-8 by human mammary gland epithelial cells

Palkowetz, K. H., Royer, C. L., Garofalo, R., Rudloff, H. E., Schmalstieg, F. C., & Goldman, A. S. (1994) · Journal of Reproductive Immunology · doi:10.1016/0165-0378(93)00867-s · Cited by 88 · see citing works

The mother-offspring dyad and the immune system

La, H. (2000) · Acta Paediatrica · doi:10.1111/j.1651-2227.2000.tb01325.x · Cited by 87 · see citing works

Tumor-associated eosinophilic infiltrate of cervical cancer is indicative for a less effective immune response

van Driel, W. J., Hogendoorn, P. C. W., Jansen, F. W., Zwinderman, A. H., Trimbos, J. B., & Fleuren, G. J. (1996) · Human Pathology · doi:10.1016/s0046-8177(96)90216-6 · Cited by 86 · see citing works

3T3-L1 Adipocytes promote the growth of mammary epithelium

Levine, J., & Stockdale, F. E. (1984) · Experimental Cell Research · doi:10.1016/0014-4827(84)90361-6 · Cited by 82 · see citing works

Novel expression pattern of a new member of the MIP-1 family of cytokine-like genes.

Orlofsky, A., Berger, M. S., & Prystowsky, M. B. (1991) · Cell Regulation · doi:10.1091/mbc.2.5.403 · Cited by 78 · see citing works

Colony-Stimulating Factor 1 Regulation of Neuroendocrine Pathways that Control Gonadal Function in Mice

Cohen, P. E., Zhu, L., Nishimura, K., & Pollard, J. W. (2002) · Endocrinology · doi:10.1210/endo.143.4.8754 · Cited by 76 · see citing works

Lumen formation in the developing mouse mammary gland

Hogg, N., Harrison, C. J., & Tickle, C. (1983) · Development · doi:10.1242/dev.73.1.39 · Cited by 75 · see citing works

Tumour-stromal interactions. Role of the stroma in mammary development.

Silberstein, G. B. (2001) · Breast Cancer Research · doi:10.1186/bcr299 · Cited by 74 · see citing works

Protein Tyrosine Phosphatase φ Regulates Paxillin Tyrosine Phosphorylation and Mediates Colony-Stimulating Factor 1-Induced Morphological Changes in Macrophages

Pixley, F. J., Lee, P. S. W., Condeelis, J. S., & Stanley, E. R. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.5.1795-1809.2001 · Cited by 73 · see citing works

Tumor necrosis factor-alpha: a multifunctional regulator of mammary gland development.

Varela, L. M., & Ip, M. M. (1996) · Endocrinology · doi:10.1210/endo.137.11.8895364 · Cited by 73 · see citing works

Regulation of rat mammary epithelial cell proliferation and differentiation by tumor necrosis factor-alpha.

Ip, M. M., Shoemaker, S. F., & Darcy, K. M. (1992) · Endocrinology · doi:10.1210/endo.130.5.1572296 · Cited by 70 · see citing works

Growth of normal and neoplastic mouse mammary epithelial cells in primary culture: stimulation by conditioned medium from mouse mammary fibroblasts.

Enami, J., Enami, S., & Koga, M. (1983) · PubMed · Cited by 67 · see citing works

Identification of Macrophage Colony-Stimulating Factor in Human Milk and Mammary Gland Epithelial Cells

Hara, T., Irie, K., Saito, S., Ichijo, M., Yamada, M., Yanai, N., & Miyazaki, S. (1995) · Pediatric Research · doi:10.1203/00006450-199504000-00009 · Cited by 56 · see citing works

The Role of CSF‐1 in Normal and Neoplastic Breast Physiology

Sapi, E., & Kacinski, B. M. (1999) · Proceedings of The Society for Experimental Biology and Medicine · doi:10.1046/j.1525-1373.1999.d01-1.x · Cited by 54 · see citing works

Leucocytes of sheep colostrum, milk and involution secretion, with particular reference to ultrastructure and lymphocyte sub-populations

Lee, C.-S., & Outteridge, P. M. (1981) · Journal of Dairy Research · doi:10.1017/s0022029900021646 · Cited by 51 · see citing works

Molecular cloning and functional characterization of a novel member of the C-C chemokine family

Hara, T., Bacon, K. B., Cho, L., Yoshimura, A., Morikawa, Y., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., Schall, T. J., & Miyajima, A. (1995) · The Journal of Immunology · doi:10.4049/jimmunol.155.11.5352 · Cited by 51 · see citing works

Leucocyte phenotypes in involuting and fully involuted mammary glandular tissues and secretions of sheep

Tatarczuch, L., Philip, C. J., Bischof, R. J., & Lee, C. S. (2000) · Journal of Anatomy · doi:10.1046/j.1469-7580.2000.19630313.x · Cited by 39 · see citing works

Occult deposition of eosinophil peroxidase in a subset of human breast carcinomas.

Samoszuk, M. K., Nguyen, V., Gluzman, I., & Pham, J. H. (1996) · Europe PMC (PubMed Central) · Cited by 38 · see citing works

Cellular immunity in the mammary gland with particular reference to T, B lymphocytes and macrophages.

Outteridge, P. M., & Cs, L. (1981) · PubMed · Cited by 38 · see citing works

Effect of tumour associated tissue eosinophilia on survival of women with stage IB carcinoma of the uterine cervix.

Bethwaite, P., Holloway, L., Yeong, M., & Thornton, A. (1993) · Journal of Clinical Pathology · doi:10.1136/jcp.46.11.1016 · Cited by 37 · see citing works

Molecular Cloning and Functional Characterization of Human MIP-1δ, a New C–C Chemokine Related to Mouse CCF-18 and C10

Wang, W., Bacon, K. B., Oldham, E. R., & Schall, T. J. (1998) · Journal of Clinical Immunology · doi:10.1023/a:1020535106684 · Cited by 36 · see citing works

Lymphocyte Homing and Ig Secretion in the Murine Mammary Gland

van der Feltz, M. J. M., de Groot, N., Bayley, J.-P., Lee, S. H., Verbeet, M. P., & Boer, H. A. D. (2001) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.2001.00933.x · Cited by 36 · see citing works

Expression of CSF-I and CSF-I Receptor by Normal Lactating Mammary Epithelial Cells

Sapi, E., Flick, M. B., Rodov, S., Carter, D., & Kacinski, B. M. (1998) · Journal of the Society for Gynecologic Investigation · doi:10.1016/s1071-5576(97)00108-1 · Cited by 36 · see citing works

Neutral proteinase expression by human mononuclear phagocytes: a prominent role of cellular differentiation.

Welgus, H. G., Senior, R. M., Parks, W. C., Kahn, A. J., Ley, T. J., Shapiro, S. D., & Campbell, E. J. (1992) · PubMed · Cited by 36 · see citing works

New marker for blood vessels in human ovarian and endometrial cancers.

Samoszuk, M. K., Lin, F., Rim, P., & Strathearn, G. (1996) · PubMed · Cited by 29 · see citing works

THE CHEMOKINE C10: IMMUNOLOGICAL AND FUNCTIONAL ANALYSIS OF THE SEQUENCE ENCODED BY THE NOVEL SECOND EXON

Berger, M. S., Taub, D. D., Orlofsky, A., Kleyman, T. R., Coupaye-Gerard, B., Eisner, D., & Cohen, S. A. (1996) · Cytokine · doi:10.1006/cyto.1996.0060 · Cited by 29 · see citing works

The Role of CSF-1 in Normal and Neoplastic Breast Physiology

Sapi, E., & Kacinski, B. M. (1999) · Experimental Biology and Medicine · doi:10.3181/00379727-220-44337 · Cited by 28 · see citing works

Light and Electron Microscopy of Cells in Pig Colostrum, Milk and Involution Secretion

Lee, C. S., McCauley, I., & Hartmann, P. E. (1983) · Cells Tissues Organs · doi:10.1159/000145734 · Cited by 24 · see citing works

SUSTAINED HIGH-LEVEL PRODUCTION OF MURINE CHEMOKINE C10 DURING CHRONIC INFLAMMATION

Wu, Y., Prystowsky, M. B., & Orlofsky, A. (1999) · Cytokine · doi:10.1006/cyto.1998.0436 · Cited by 23 · see citing works

Effects of dietary fat on the growth of normal, preneoplastic and neoplastic mammary epithelial cells in vivo and in vitro

Carrington, C. A., & Hosick, H. L. (1985) · Journal of Cell Science · doi:10.1242/jcs.75.1.269 · Cited by 23 · see citing works

Identification of a novel β-chemokine, MEC, down-regulated in primary breast tumors

Mickanin, C., Bhatia, U., & Labow, M. (2001) · International Journal of Oncology · doi:10.3892/ijo.18.5.939 · Cited by 18 · see citing works

Defective interleukin six expression and responsiveness in human mammary cells transformed by an adeno 5/SV40 hybrid virus

Basolo, F., Fiore, L., Calvo, S., Falcone, V., Conaldi, P. G., Fontanini, G., Caligo, M. A., Merlo, G. R., Gluzman, Y., & Toniolo, A. (1996) · British Journal of Cancer · doi:10.1038/bjc.1996.258 · Cited by 13 · see citing works

IgE, Reed-Sternberg Cells, and Eosinophilia in Hodgkin's Disease

Samoszuk, M. K., & Ramzi, E. (1993) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.3109/10428199309148528 · Cited by 12 · see citing works

STUDIES ON THE INFLAMMATORY RESPONSE DURING INVOLUTION OF THE OVINE MAMMARY GLAND

Colditz, I. G. (1988) · Quarterly Journal of Experimental Physiology · doi:10.1113/expphysiol.1988.sp003152 · Cited by 10 · see citing works

Mast cells in the mouse mammary gland--correlation with the development of lactiferous structures.

Szewczyk, G., Szukiewicz, D., Zaczek, R., & Maślińska, D. (2000) · PubMed · Cited by 9 · see citing works

Untitled work

(1997) · doi:10.1002/(sici)1098-2795(199701)46:1

Tumour-educated macrophages promote tumour progression and metastasis

Pollard, J. W. (2004) · Nature reviews. Cancer · doi:10.1038/nrc1256 · Cited by 3,365 · see citing works

Hypoalbuminemia: Pathogenesis and Clinical Significance

Soeters, P. B., Wolfe, R. R., & Shenkin, A. (2019) · Journal of Parenteral and Enteral Nutrition · doi:10.1002/jpen.1451 · Cited by 1,448 · see citing works

The eosinophil

Rothenberg, M. E., & Hogan, S. P. (2006) · Annual Review of Immunology · doi:10.1146/annurev.immunol.24.021605.090720 · Cited by 1,356 · see citing works

Identification of discrete tumor-induced myeloid-derived suppressor cell subpopulations with distinct T cell–suppressive activity

Movahedi, K., Guilliams, M., den Bossche, J. V., den Bergh, R. V., Gysemans, C. A., Beschin, A., BAETSELIER, P. D., & Ginderachter, J. A. V. (2008) · Blood · doi:10.1182/blood-2007-07-099226 · Cited by 1,234 · see citing works

Trophic macrophages in development and disease

Pollard, J. W. (2009) · Nature Reviews Immunology · doi:10.1038/nri2528 · Cited by 1,178 · see citing works

Progression to Malignancy in the Polyoma Middle T Oncoprotein Mouse Breast Cancer Model Provides a Reliable Model for Human Diseases

Lin, E. Y., Jones, J. G., Li, P., Zhu, L., Whitney, K. D., Muller, W. J., & Pollard, J. W. (2003) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)63568-7 · Cited by 1,109 · see citing works

A Distinct Macrophage Population Mediates Metastatic Breast Cancer Cell Extravasation, Establishment and Growth

Qian, B., Deng, Y., Im, J. H., Muschel, R. J., Zou, Y., Li, J., Lang, R. A., & Pollard, J. W. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006562 · Cited by 664 · see citing works

Metabolism of tissue macrophages in homeostasis and pathology

Wculek, S. K., Dunphy, G., Heras-Murillo, I., Mastrangelo, A., & Sancho, D. (2022) · Cellular & Molecular Immunology · doi:10.1038/s41423-021-00791-9 · Cited by 501 · see citing works

A Renewable Tissue Resource of Phenotypically Stable, Biologically and Ethnically Diverse, Patient-Derived Human Breast Cancer Xenograft Models

Zhang, X., Claerhout, S., Prat, A., Dobrolecki, L. E., Petrovic, I., Lai, Q., Landis, M. D., Wiechmann, L., Schiff, R., Giuliano, M., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-4081 · Cited by 483 · see citing works

Functions of tissue-resident eosinophils

Weller, P. F., & Spencer, L. A. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.95 · Cited by 480 · see citing works

Key stages in mammary gland development: The cues that regulate ductal branching morphogenesis

Sternlicht, M. D. (2005) · Breast Cancer Research · doi:10.1186/bcr1368 · Cited by 424 · see citing works

Macrophages define the invasive microenvironment in breast cancer

Pollard, J. W. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.1107762 · Cited by 414 · see citing works

Macrophages orchestrate breast cancer early dissemination and metastasis

Linde, N., Casanova-Acebes, M., Sosa, M. S., Mortha, A., Rahman, A. H., Farias, E., Harper, K. L., Tardio, E., Reyes-Torres, I., Jones, J. G., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-02481-5 · Cited by 416 · see citing works

Chapter 3 Biology of the Eosinophil

Blanchard, C., & Rothenberg, M. E. (2009) · Advances in immunology · doi:10.1016/s0065-2776(08)01003-1 · Cited by 344 · see citing works

Eosinophils in health and disease: the LIAR hypothesis

Lee, J. J., Jacobsen, E. A., McGarry, M. P., Schleimer, R. P., & Lee, N. A. (2010) · Clinical & Experimental Allergy · doi:10.1111/j.1365-2222.2010.03484.x · Cited by 335 · see citing works

Macrophage Polarization in Health and Disease

Cassetta, L., Cassol, E., & Poli, G. (2011) · The Scientific World JOURNAL · doi:10.1100/2011/213962 · Cited by 335 · see citing works

Amphiregulin is an essential mediator of estrogen receptor α function in mammary gland development

Ciarloni, L., Mallepell, S., & Brisken, C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611647104 · Cited by 316 · see citing works

Hormonal and local control of mammary branching morphogenesis

Sternlicht, M. D., Kouros‐Mehr, H., Lu, P., & Werb, Z. (2006) · Differentiation · doi:10.1111/j.1432-0436.2006.00105.x · Cited by 303 · see citing works

Patient-derived xenograft (PDX) models in basic and translational breast cancer research

Dobrolecki, L. E., Airhart, S., Alférez, D., Aparicio, S. A. J. R., Behbod, F., Bentires‐Alj, M., Brisken, C., Bult, C. J., Cai, S., Clarke, R. B., et al. (2016) · Cancer and Metastasis Reviews · doi:10.1007/s10555-016-9653-x · Cited by 261 · see citing works

Inflammatory cells contribute to the generation of an angiogenic phenotype in pancreatic ductal adenocarcinoma

Esposito, I., Menicagli, M., Funel, N., Bergmann, F., Boggi, U., Mosca, F., Bevilacqua, G., & Campani, D. (2004) · Journal of Clinical Pathology · doi:10.1136/jcp.2003.014498 · Cited by 257 · see citing works

Eosinophils in innate immunity: an evolving story

Shamri, R., Xenakis, J. J., & Spencer, L. A. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1049-6 · Cited by 256 · see citing works

Gene Expression Analysis of Macrophages That Facilitate Tumor Invasion Supports a Role for Wnt-Signaling in Mediating Their Activity in Primary Mammary Tumors

Ojalvo, L. S., Whittaker, C. A., Condeelis, J. S., & Pollard, J. W. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0902360 · Cited by 239 · see citing works

High-Density Gene Expression Analysis of Tumor-Associated Macrophages from Mouse Mammary Tumors

Ojalvo, L. S., King, W., Cox, D., & Pollard, J. W. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080676 · Cited by 221 · see citing works

Tissue injury and repair in the female human reproductive tract

Salamonsen, L. A. (2003) · Reproduction · doi:10.1530/rep.0.1250301 · Cited by 217 · see citing works

Recent Advances in Type-2-Cell-Mediated Immunity: Insights from Helminth Infection

Harris, N. L., & Loke, P. (2017) · Immunity · doi:10.1016/j.immuni.2017.11.015 · Cited by 211 · see citing works

Aging-Associated Alterations in Mammary Epithelia and Stroma Revealed by Single-Cell RNA Sequencing

Li, C. M.-C., Shapiro, H., Tsiobikas, C., Selfors, L. M., Chen, H., Rosenbluth, J., Moore, K., Gupta, K. P., Gray, G. K., Oren, Y., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108566 · Cited by 184 · see citing works

Analysing the eosinophil cationic protein - a clue to the function of the eosinophil granulocyte

Byström, J., Amin, K., & Bishop‐Bailey, D. (2011) · Respiratory Research · doi:10.1186/1465-9921-12-10 · Cited by 208 · see citing works

Leukocytes in Mammary Development and CancerPreprint

Coussens, L. M., & Pollard, J. W. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003285 · Cited by 209 · see citing works

Tissue-resident ductal macrophages survey the mammary epithelium and facilitate tissue remodelling

Dawson, C. A., Pal, B., Vaillant, F., Gandolfo, L. C., Liu, Z.-Y., Blériot, C., Ginhoux, F., Smyth, G., Lindeman, G., Mueller, S. N., et al. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-0505-0 · Cited by 149 · see citing works

Insulin cell mass is altered in Csf1 op /Csf1 op macrophage-deficient mice

Banaei-Bouchareb, L., Gouon–Evans, V., Samara‐Boustani, D., Castellotti, M. C., Czernichow, P., Pollard, J. W., & Polak, M. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.1103591 · Cited by 170 · see citing works

Mammary Gland Involution as a Multi-step Process

Stein, T., Salomonis, N., & Gusterson, B. A. (2007) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-007-9035-7 · Cited by 170 · see citing works

The Role of the Immune System Beyond the Fight Against Infection

Sattler, S. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-57613-8_1 · Cited by 167 · see citing works

Tissue-resident versus monocyte-derived macrophages in the tumor microenvironment

Lahmar, Q., Keirsse, J., Laoui, D., Movahedi, K., Overmeire, E. V., & Ginderachter, J. A. V. (2015) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2015.06.009 · Cited by 151 · see citing works

Shaping eosinophil identity in the tissue contexts of development, homeostasis, and disease

Abdala‐Valencia, H., Coden, M. E., Chiarella, S. E., Jacobsen, E. A., Bochner, B. S., Lee, J. J., & Berdnikovs, S. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.1mr1117-442rr · Cited by 144 · see citing works

Conditional deletion of the colony stimulating factor-1 receptor (c-fms proto-oncogene) in mice

Li, J., Chen, K., Zhu, L., & Pollard, J. W. (2006) · genesis · doi:10.1002/dvg.20219 · Cited by 128 · see citing works

Resident macrophages influence stem cell activity in the mammary gland

Gyorki, D. E., Asselin-Labat, M.-L., van Rooijen, N., Lindeman, G. J., & Visvader, J. E. (2009) · Breast Cancer Research · doi:10.1186/bcr2353 · Cited by 121 · see citing works

Evaluation of Prenatal Exposure to Bisphenol Analogues on Development and Long-Term Health of the Mammary Gland in Female Mice

Tucker, D. K., Bouknight, S. H., Brar, S. S., Kissling, G. E., & Fenton, S. E. (2018) · Environmental Health Perspectives · doi:10.1289/ehp3189 · Cited by 117 · see citing works

Small intestinal resident eosinophils maintain gut homeostasis following microbial colonization

Ignácio, A., Shah, K., Bernier‐Latmani, J., Köller, Y., Coakley, G., Moyat, M., Hamelin, R., Armand, F., Wong, N. C., Ramay, H. R., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.05.014 · Cited by 119 · see citing works

The Utility of Immunohistochemistry for the Identification of Hematopoietic and Lymphoid Cells in Normal Tissues and Interpretation of Proliferative and Inflammatory Lesions of Mice and Rats

Rehg, J. E., Bush, D. A., & Ward, J. M. (2012) · Toxicologic Pathology · doi:10.1177/0192623311430695 · Cited by 117 · see citing works

Mast cells contribute to the stromal microenvironment in mammary gland branching morphogenesis

Lilla, J. N., & Werb, Z. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.10.021 · Cited by 115 · see citing works

Correction: Lactation Defect with Impaired Secretory Activation in AEBP1-Null Mice

Zhang, L., Reidy, S. P., Bogachev, O., Hall, B. K., & Majdalawieh, H.-S. A. (2011) · PLoS ONE · doi:10.1371/annotation/4056d03c-20ed-4eca-9568-3e9400e2312e · Cited by 111 · see citing works

Contribution of CXCL12 secretion to invasion of breast cancer cells

Boimel, P. J., Смирнова, Т. А., Zhou, Z. N., Wyckoff, J. B., Park, H., Coniglio, S. J., Qian, B., Stanley, E. R., Cox, D., Pollard, J. W., et al. (2012) · Breast Cancer Research · doi:10.1186/bcr3108 · Cited by 110 · see citing works

Adaptive Immune Regulation of Mammary Postnatal Organogenesis

Plaks, V., Boldajipour, B. A., Linnemann, J. R., Nguyen, N. H., Kersten, K., Wolf, Y., Casbon, A.-J., Kong, N., van den Bijgaart, R. J. E., Sheppard, D., et al. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.07.015 · Cited by 107 · see citing works

Understanding the Biology of Self-Renewing Macrophages

Röszer, T. (2018) · Cells · doi:10.3390/cells7080103 · Cited by 91 · see citing works

Inflaming sex differences in mood disorders

Rainville, J. R., & Hodes, G. E. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0124-7 · Cited by 106 · see citing works

Common Molecular Mechanisms of Mammary Gland Development and Breast Cancer

Lanigan, F. T., O’Connor, D. P., Martin, F., & Gallagher, W. M. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7386-2 · Cited by 105 · see citing works

Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milkPreprint

Wan, Y., Saghatelian, A., Chong, L.-W., Zhang, C.-L., Cravatt, B. F., & Evans, R. M. (2007) · Genes & Development · doi:10.1101/gad.1567207 · Cited by 103 · see citing works

Lactation and Its Hormonal Control

Anderson, S., MacLean, P., McManaman, J., & Neville, M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397175-3.00046-6 · Cited by 68 · see citing works

Pubertal Mammary Gland Development: Insights from Mouse Models

Howlin, J., McBryan, J., & Martin, F. (2006) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-006-9024-2 · Cited by 97 · see citing works

Tumor-associated macrophage heterogeneity is driven by tissue territories in breast cancer

Laviron, M., Petit, M., Weber-Delacroix, E., Combes, A. J., Arkal, A. R., Barthélémy, S., Courau, T., Hume, D. A., Combadière, C., Krummel, M. F., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110865 · Cited by 95 · see citing works

The emerging roles of eosinophils in mucosal homeostasis

Shah, K., Ignácio, A., McCoy, K. D., & Harris, N. L. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-0281-y · Cited by 91 · see citing works

The Breast Cancer and the Environment Research Centers: Transdisciplinary Research on the Role of the Environment in Breast Cancer Etiology

Hiatt, R. A., Haslam, S. Z., & Osuch, J. R. (2009) · Environmental Health Perspectives · doi:10.1289/ehp.0800120 · Cited by 90 · see citing works

Immunotherapy in breast cancer: Current status and future directions

(2019) · Advances in Cancer Research · doi:10.1016/bs.acr.2019.03.006 · Cited by 109 · see citing works

Regulatory eosinophils induce the resolution of experimental arthritis and appear in remission state of human rheumatoid arthritis

Andreev, D., Liu, M., Kachler, K., Perez, M. L., Kirchner, P., Koelle, J., Gießl, A., Rauber, S., Song, R., Aust, O., et al. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-218902 · Cited by 88 · see citing works

Macrophages: Regulators of the Inflammatory Microenvironment during Mammary Gland Development and Breast Cancer

Brady, N. J., Chuntova, P., & Schwertfeger, K. L. (2016) · Mediators of Inflammation · doi:10.1155/2016/4549676 · Cited by 86 · see citing works

Effects of milk fermented by Lactobacillus helveticus R389 on immune cells associated to mammary glands in normal and a breast cancer model.

de Moreno de LeBlanc, A., Matar, C., Thériault, C., & Perdigón, G. (2005) · Immunobiology · doi:10.1016/j.imbio.2005.05.024 · Cited by 85 · see citing works

Kinetics of milk lipid droplet transport, growth, and secretion revealed by intravital imaging: lipid droplet release is intermittently stimulated by oxytocin

Masedunskas, A., Chen, Y., Stussman, R., Weigert, R., & Mather, I. H. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-11-0776 · Cited by 84 · see citing works

Assessing serum cytokine profiles in breast cancer patients receiving a HER2/neu vaccine using Luminex® technology

Dehqanzada, Z. A., Storrer, C. E., Hueman, M. T., Foley, R. J., Harris, K. A., Jama, Y. H., Shriver, C. D., Ponniah, S., & Peoples, G. E. (2007) · Oncology Reports · doi:10.3892/or.17.3.687 · Cited by 82 · see citing works

Mucosal Immunity in the Female Murine Mammary Gland

Betts, C. B., Pennock, N. D., Caruso, B. P., Ruffell, B., Borges, V. F., & Schedin, P. S. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1800023 · Cited by 77 · see citing works

Immune Cell Location and Function During Post-Natal Mammary Gland Development

Reed, J. R., & Schwertfeger, K. L. (2010) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-010-9188-7 · Cited by 76 · see citing works

Nanoparticle-Based Magnetic Resonance Imaging on Tumor-Associated Macrophages and Inflammation

Serkova, N. J. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00590 · Cited by 76 · see citing works

Comparative Aspects of Mammary Gland Development and Homeostasis

Capuco, A. V., & Ellis, S. E. (2013) · Annual Review of Animal Biosciences · doi:10.1146/annurev-animal-031412-103632 · Cited by 75 · see citing works

Macrophages in Breast Cancer: Do Involution Macrophages Account for the Poor Prognosis of Pregnancy-Associated Breast Cancer?

O’Brien, J., & Schedin, P. S. (2009) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-009-9118-8 · Cited by 73 · see citing works

Deciphering sex differences in the immune system and depression

Rainville, J. R., Tsyglakova, M., & Hodes, G. E. (2017) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.12.004 · Cited by 69 · see citing works

Next Stop, the Twilight Zone: Hedgehog Network Regulation of Mammary Gland Development

Lewis, M. T., & Veltmaat, J. M. (2004) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1023/b:jomg.0000037160.24731.35 · Cited by 71 · see citing works

Myeloid cell trafficking and tumor angiogenesis

Schmid, M. C., & Varner, J. A. (2006) · Cancer Letters · doi:10.1016/j.canlet.2006.09.002 · Cited by 70 · see citing works

Mammary Gland Reprogramming: Metalloproteinases Couple Form with FunctionPreprint

Khokha, R., & Werb, Z. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004333 · Cited by 65 · see citing works

Developmental Stage-Specific Distribution of Macrophages in Mouse Mammary Gland

Stewart, T. A., Hughes, K., Hume, D. A., & Davis, F. M. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00250 · Cited by 64 · see citing works

Relationships Among Microbial Communities, Maternal Cells, Oligosaccharides, and Macronutrients in Human Milk

Williams, J. E., Price, W. J., Shafii, B., Yahvah, K. M., Bode, L., McGuire, M. A., & McGuire, M. K. (2017) · Journal of Human Lactation · doi:10.1177/0890334417709433 · Cited by 63 · see citing works

Prolactin: A hormone with diverse functions from mammary gland development to cancer metastasis

Atıcı, Ö. K., Govindrajan, N., Lopetegui-Gonzalez, I., & Shemanko, C. S. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.10.005 · Cited by 63 · see citing works

Mammary Gland Macrophages: Pleiotropic Functions in Mammary Development

Schwertfeger, K. L., Rosen, J. M., & Cohen, D. A. (2006) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-006-9028-y · Cited by 61 · see citing works

Critical Roles for Macrophages in Islet Angiogenesis and Maintenance During Pancreatic Degeneration

Tessem, J. S., Jensen, J. N., Pelli, H., Dai, X.-M., Zong, X.-H., Stanley, E. R., Jensen, J. N., & DeGregori, J. V. (2008) · Diabetes · doi:10.2337/db07-1577 · Cited by 57 · see citing works

High TGF-β signature predicts immunotherapy resistance in gynecologic cancer patients treated with immune checkpoint inhibition

Ni, Y., Soliman, A. S. A., Joehlin-Price, A. S., Rose, P. G., Vlad, A., Edwards, R. P., & Mahdi, H. (2021) · npj Precision Oncology · doi:10.1038/s41698-021-00242-8 · Cited by 57 · see citing works

A transient microenvironment loaded mainly with macrophages in the early developing human pancreas

Banaei-Bouchareb, L., Peuchmaur, M. M., Czernichow, P., & Polak, M. (2006) · Journal of Endocrinology · doi:10.1677/joe.1.06225 · Cited by 56 · see citing works

Epithelial-Specific and Stage-Specific Functions of Insulin-Like Growth Factor-I during Postnatal Mammary Development

Loladze, A. V., Stull, M. A., Rowzee, A. M., DeMarco, J., Lantry, J. H., Rosen, C. J., LeRoith, D., Wagner, K., Hennighausen, L. G., & Wood, T. L. (2006) · Endocrinology · doi:10.1210/en.2006-0427 · Cited by 54 · see citing works

Pubertal high fat diet: effects on mammary cancer development

Zhao, Y. M., Tan, Y. S., Aupperlee, M. D., Langohr, I. M., Kirk, E. L., Troester, M. A., Schwartz, R. C., & Haslam, S. Z. (2013) · Breast Cancer Research · doi:10.1186/bcr3561 · Cited by 53 · see citing works

Monocyte transplantation for neural and cardiovascular ischemia repair

Sanberg, P. R., Park, D., Kuzmin‐Nichols, N., Cruz, E., Hossne, N. A., Buffolo, Ê., & Willing, A. E. (2009) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2009.00903.x · Cited by 51 · see citing works

Eosinophils and Lung Cancer: From Bench to Bedside

Sibille, A., Corhay, J.-L., Louis, R. E., Ninane, V., Jérusalem, G., & Duysinx, B. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23095066 · Cited by 48 · see citing works

CCR2 deficiency leads to increased eosinophils, alternative macrophage activation, and type 2 cytokine expression in adipose tissue

Bolus, W. R., Gutierrez, D. A., Kennedy, A. J., Anderson‐Baucum, E. K., & Hasty, A. H. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.3hi0115-018r · Cited by 48 · see citing works

Comparative mammary gland postnatal development and tumourigenesis in the sheep, cow, cat and rabbit: Exploring the menagerie

Hughes, K. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.09.010 · Cited by 48 · see citing works

Expression pattern of four membrane‐type matrix metalloproteinases in the normal and diseased mouse mammary gland

Szabova, L., Yamada, S. S., Birkedal‐Hansen, H., & Holmbeck, K. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20385 · Cited by 48 · see citing works

Mammary gland development—It’s not just about estrogen

Berryhill, G. E., Trott, J. F., & Hovey, R. C. (2015) · Journal of Dairy Science · doi:10.3168/jds.2015-10105 · Cited by 47 · see citing works

Expression of the Insulin-Like Growth Factor Binding Proteins during Postnatal Development of the Murine Mammary Gland

Allar, M. A., & Wood, T. L. (2004) · Endocrinology · doi:10.1210/en.2003-1641 · Cited by 46 · see citing works

Deletion of cyclooxygenase 2 in mouse mammary epithelial cells delays breast cancer onset through augmentation of type 1 immune responses in tumors

Markosyan, N., Chen, E. P., Ndong, V. N., Yao, Y., Sterner, C. J., Chodosh, L. A., Lawson, J. A., FitzGerald, G. A., & Smyth, E. M. (2011) · Carcinogenesis · doi:10.1093/carcin/bgr134 · Cited by 45 · see citing works

Macrophages in Renal Development, Injury, and Repair

Williams, T. M., Little, M. H., & Ricardo, S. D. (2010) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2010.03.011 · Cited by 44 · see citing works

Breast cancer mammospheres secrete Adrenomedullin to induce lipolysis and browning of adjacent adipocytes

Paré, M., Darini, C., Yao, X., Chignon‐Sicard, B., Rekima, S., Lachambre, S., Virolle, V., Aguilar‐Mahecha, A., Basik, M., Dani, C., et al. (2020) · BMC Cancer · doi:10.1186/s12885-020-07273-7 · Cited by 44 · see citing works

An “elite hacker”: breast tumors exploit the normal microenvironment program to instruct their progression and biological diversity

Boudreau, A., van't Veer, L. J., & Bissell, M. J. (2012) · Cell Adhesion & Migration · doi:10.4161/cam.20880 · Cited by 43 · see citing works

p120-catenin is essential for terminal end bud function and mammary morphogenesis

Kurley, S. J., Bierie, B., Carnahan, R. H., Lobdell, N. A., Davis, M. A., Hofmann, I., Moses, H. L., Muller, W. J., & Reynolds, A. B. (2012) · Development · doi:10.1242/dev.072769 · Cited by 43 · see citing works

Emerging Evidence for Pleiotropism of Eosinophils

Rodrigo-Muñoz, J. M., Gil‐Martínez, M., Sastre, B., & del Pozo, V. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137075 · Cited by 46 · see citing works

The Eosinophil in Health and Disease: from Bench to Bedside and Back

Liao, W., Long, H., Chang, C., & Lu, Q.-J. (2016) · Clinical reviews in allergy and immunology · doi:10.1007/s12016-015-8507-6 · Cited by 47 · see citing works

Role of Prolactin in Promotion of Immune Cell Migration into the Mammary Gland

Dill, R., & Walker, A. M. (2016) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-016-9369-0 · Cited by 42 · see citing works

Apocrine Cysts of the Breast

Celis, J. E., Gromov, P., Moreira, J. M. A., Cabezón, T., Friis, E., Vejborg, I., Proess, G., Rank, F. E., & Gromova, I. (2005) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m500348-mcp200 · Cited by 42 · see citing works

Identification of macrophages in normal and injured mouse tissues using reporter lines and antibodies

Chen, B., Li, R., Kubota, A., Alex, L., & Frangogiannis, N. G. (2022) · Scientific Reports · doi:10.1038/s41598-022-08278-x · Cited by 42 · see citing works

CSF-1R Signaling in Health and Disease: A Focus on the Mammary Gland

Dwyer, A. R., & Pixley, F. J. (2014) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-014-9320-1 · Cited by 40 · see citing works

Motility cues in the tumor microenvironment

Quaranta, V. (2002) · Differentiation · doi:10.1046/j.1432-0436.2002.700912.x · Cited by 40 · see citing works

Stromal Fibroblasts and the Immune Microenvironment: Partners in Mammary Gland Biology and Pathology?

Unsworth, A., Anderson, R. L., & Britt, K. L. (2014) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-014-9326-8 · Cited by 38 · see citing works

Dynamic architectural interplay between leucocytes and mammary epithelial cells

Hitchcock, J. R., Hughes, K., Harris, O. B., & Watson, C. J. (2019) · FEBS Journal · doi:10.1111/febs.15126 · Cited by 38 · see citing works

Eosinophils as Major Player in Type 2 Inflammation: Autoimmunity and Beyond

Folci, M., Ramponi, G., Arcari, I., Zumbo, A., & Brunetta, E. (2021) · Advances in experimental medicine and biology · doi:10.1007/5584_2021_640 · Cited by 37 · see citing works

Changes in Immune Cell Types with Age in Breast are Consistent with a Decline in Immune Surveillance and Increased Immunosuppression

Zirbes, A., Joseph, J., Lopez, J. C., Sayaman, R. W., Basam, M., Seewaldt, V. L., & LaBarge, M. A. (2021) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-021-09495-2 · Cited by 36 · see citing works

Ptch1is required locally for mammary gland morphogenesis and systemically for ductal elongation

Moraes, R., Chang, H., Harrington, N., Landua, J. D., Prigge, J. T., Lane, T. F., Wainwright, B. J., Hamel, P. A., & Lewis, M. T. (2009) · Development · doi:10.1242/dev.023994 · Cited by 36 · see citing works

Review Requirement of macrophages and eosinophils and their cytokines/chemokines for mammary gland development

Gouon–Evans, V., Lin, E. Y., & Pollard, J. W. (2002)

Postnatal mammary gland development requires macrophages and eosinophils

Gouon–Evans, V., Rothenberg, M. E., & Pollard, J. W. (2000) · Development · doi:10.1242/dev.127.11.2269 · Cited by 463 · see citing works

Colony Stimulating Factor-1 Is Required to Recruit Macrophages into the Mammary Gland to Facilitate Mammary Ductal Outgrowth

Nguyen, A., & Pollard, J. W. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0669 · Cited by 125 · see citing works

Cytokine Networks That Mediate Epithelial Cell-Macrophage Crosstalk in the Mammary Gland: Implications for Development and Cancer

Sun, X., & Ingman, W. V. (2014) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-014-9319-7 · Cited by 33 · see citing works

Functional Mechanisms of the Macrophage Growth Factor (CSF-1) and Tumor-Associated Macrophages in Breast Tumor Malignancy

Gouon–Evans, V. (1999) · Defense Technical Information Center (DTIC)