The expression of the receptor for advanced glycation endproducts (RAGE) is permissive for early pancreatic neoplasia
Open accessAbstract
Pancreatic cancer is an almost uniformly lethal disease, characterized by late diagnosis, early metastasis, resistance to chemotherapy, and early mutation of the Kras oncogene. Here we show that the receptor for advanced glycation endproducts (RAGE) is required for the activation of interleukin 6 (IL-6)–mediated mitochondrial signal transducers and activators of transcription 3 (STAT3) signaling in pancreatic carcinogenesis. RAGE expression correlates with elevated levels of autophagy in pancreatic cancer in vivo and in vitro, and this heightened state of autophagy is required for IL-6–induced STAT3 activation. To further explore the intersection of RAGE, autophagy, and pancreatic carcinogenesis, we created a transgenic murine model, backcrossing RAGE-null mice to a spontaneous mouse model of pancreatic cancer, Pdx1-Cre : Kras G12D/+ (KC). Targeted ablation of Rage in KC mice delayed neoplasia development, decreased levels of autophagy, and inhibited mitochondrial STAT3 activity and subsequent ATP production. Our results suggest a critical role for RAGE expression in the earliest stages of pancreatic carcinogenesis, potentially acting as the “autophagic switch,” regulating mitochondrial STAT3 signaling.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
RAGE is highly upregulated in metastatic and aggressive breast, ovarian, and pancreatic cancer, acting as a promotor of the progression of premalignant precursors to invasive carcinoma.
“RAGE is highly upregulated in metastatic and aggressive breast, ovarian, and pancreatic cancer, acting as a promotor of the progression of premalignant precursors to invasive carcinoma88,89.”
From Advanced glycation end products (AGEs) and other adducts in aging-related diseases and alcohol-mediated tissue injury (2021) · cites this paper as [88]
Cites
Methods in Mammalian Autophagy Research
Mizushima, N., Yoshimori, T., & Levine, B. (2010) · Cell · doi:10.1016/j.cell.2010.01.028 · Cited by 4,497 · see citing works
STATs in cancer inflammation and immunity: a leading role for STAT3
Yu, H., Pardoll, D., & Jove, R. (2009) · Nature reviews. Cancer · doi:10.1038/nrc2734 · Cited by 4,383 · see citing works
Siegel, R. L., Ward, E., Brawley, O. W., & Jemal, A. (2011) · CA A Cancer Journal for Clinicians · doi:10.3322/caac.20121 · Cited by 4,075 · see citing works
Induction of autophagy and inhibition of tumorigenesis by beclin 1
Liang, X. H., Jackson, S., Seaman, M., Brown, K., Kempkes, B., Hibshoosh, H., & Levine, B. (1999) · Nature · doi:10.1038/45257 · Cited by 3,347 · see citing works
The role of autophagy during the early neonatal starvation period
Kuma, A., Hatano, M., Matsui, M., Yamamoto, A., Nakaya, H., Yoshimori, T., Ohsumi, Y., Tokuhisa, T., & Mizushima, N. (2004) · Nature · doi:10.1038/nature03029 · Cited by 2,865 · see citing works
Preinvasive and invasive ductal pancreatic cancer and its early detection in the mouse
Hingorani, S. R., Petricoin, E. F., Maitra, A., Rajapakse, V., King, C., Jacobetz, M. A., Ross, S., Conrads, T. P., Veenstra, T. D., Hitt, B. A., et al. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00309-x · Cited by 2,471 · see citing works
Cancer cell metabolism: warburg and beyond
Hsu, P. P., & Sabatini, D. M. (2008) · Cell · doi:10.1016/j.cell.2008.08.021 · Cited by 2,452 · see citing works
Eaten alive: a history of macroautophagy
Yang, Z., & Klionsky, D. J. (2010) · Nature Cell Biology · doi:10.1038/ncb0910-814 · Cited by 2,096 · see citing works
Rabinowitz, J. D., & White, E. (2010) · Science · doi:10.1126/science.1193497 · Cited by 1,982 · see citing works
Pancreatic cancers require autophagy for tumor growth
Yang, S., Wang, X., Contino, G., Liesa, M., Sahin, E., Ying, H., Bause, A., Li, Y., Stommel, J. M., Dell'Antonio, G., et al. (2011) · Genes & Development · doi:10.1101/gad.2016111 · Cited by 1,498 · see citing works
HMGB1 and RAGE in Inflammation and Cancer
Sims, G. P., Rowe, D. C., Rietdijk, S. T., Herbst, R., & Coyle, A. J. (2010) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132603 · Cited by 1,436 · see citing works
Autophagy-deficient mice develop multiple liver tumors
Takamura, A., Komatsu, M., Hara, T., Sakamoto, A., Kishi, C., Waguri, S., Eishi, Y., Hino, O., Tanaka, K., & Mizushima, N. (2011) · Genes & Development · doi:10.1101/gad.2016211 · Cited by 1,342 · cited 1× · see citing works
“For example, autophagy inhibits the development of breast (27) and liver cancers (28), but it promotes the growth of pancreatic cancer (12) and BCR-Abl–associated leukemia (29).”
BackgroundActivated Ras requires autophagy to maintain oxidative metabolism and tumorigenesis
Guo, J. Y., Chen, H.-Y., Mathew, R., Fan, J., Strohecker, A. M., Karsli-Uzunbas, G., Kamphorst, J. J., Chen, G., Lemons, J. M. S., Karantza, V., et al. (2011) · Genes & Development · doi:10.1101/gad.2016311 · Cited by 1,323 · see citing works
Blockade of RAGE-amphoterin signalling suppresses tumour growth and metastases
Taguchi, A., Blood, D. C., del Toro, G., Canet, A., Lee, D. C., Qu, W., Tanji, N., Lu, Y., Lalla, E., Fu, C., et al. (2000) · Nature · doi:10.1038/35012626 · Cited by 1,217 · see citing works
The Atg12-Atg5 Conjugate Has a Novel E3-like Activity for Protein Lipidation in Autophagy
Hanada, T., Noda, N. N., Satomi, Y., Ichimura, Y., Fujioka, Y., Takao, T., Inagaki, F., & Ohsumi, Y. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.c700195200 · Cited by 1,123 · cited 1× · see citing works
“The ATG12–ATG5 conjugate has an E3-like ubiquitin ligase activity-promoting protein lipidation in autophagy (18) that is critical for the elongation of the initiating autophagosomal membrane.”
BackgroundFunction of Mitochondrial Stat3 in Cellular Respiration
Wegrzyn, J., Potla, R., Chwae, Y.-J., Sepuri, N. B. V., Zhang, Q., Koeck, T., Derecka, M., Szczepanek, K., Szelag, M., Gornicka, A., et al. (2009) · Science · doi:10.1126/science.1164551 · Cited by 1,014 · see citing works
Lesina, M., Kurkowski, M. U., Ludes, K., Rose-John, S., Treiber, M., Klöppel, G., Yoshimura, A., Reindl, W., Sipos, B., Akira, S., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.03.009 · Cited by 862 · see citing works
Mitochondrial STAT3 Supports Ras-Dependent Oncogenic Transformation
Gough, D. J., Corlett, A., Schlessinger, K., Wegrzyn, J., Larner, A. C., & Levy, D. E. (2009) · Science · doi:10.1126/science.1171721 · Cited by 716 · see citing works
Sparvero, L. J., Asafu-Adjei, D. A., Kang, R., Tang, D., Amin, N., Im, J., Rutledge, R., Lin, B., Amoscato, A. A., Zeh, H. J., et al. (2009) · Journal of Translational Medicine · doi:10.1186/1479-5876-7-17 · Cited by 625 · see citing works
Self-citationInflammation and Cancer: IL-6 and STAT3 Complete the Link
Bromberg, J., & Wang, T. C. (2009) · Cancer Cell · doi:10.1016/j.ccr.2009.01.009 · Cited by 570 · see citing works
Stat3 and MMP7 Contribute to Pancreatic Ductal Adenocarcinoma Initiation and Progression
Fukuda, A., Wang, S. C., Morris, J. P., Folias, A. E., Liou, A., Kim, G. E., Akira, S., Boucher, K., Firpo, M., Mulvihill, S., et al. (2011) · Cancer Cell · doi:10.1016/j.ccr.2011.03.002 · Cited by 531 · see citing works
Autophagy facilitates glycolysis during Ras-mediated oncogenic transformation
Lock, R., Roy, S., Kenific, C. M., Su, J. S., Salas, E., Ronen, S. M., & Debnath, J. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-06-0500 · Cited by 467 · see citing works
RAGE signaling sustains inflammation and promotes tumor development
Gebhardt, C., Riehl, A., Durchdewald, M., Németh, J., Fürstenberger, G., Müller‐Decker, K., Enk, A., Arnold, B., Bierhaus, A., Nawroth, P. P., et al. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20070679 · Cited by 380 · see citing works
Kang, R., Tang, D., Schapiro, N. E., Livesey, K. M., Farkas, A. M., Loughran, P., Bierhaus, A., Lotze, M. T., & Zeh, H. J. (2009) · Cell Death and Differentiation · doi:10.1038/cdd.2009.149 · Cited by 333 · see citing works
Self-citationHigh-Mobility Group Box 1 Is Essential for Mitochondrial Quality Control
Tang, D., Kang, R., Livesey, K. M., Kroemer, G., Billiar, T. R., Houten, B. V., Zeh, H. J., & Lotze, M. T. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.04.008 · Cited by 296 · see citing works
Self-citationAutophagy is activated in pancreatic cancer cells and correlates with poor patient outcome
Fujii, S., Mitsunaga, S., Yamazaki, M., Hasebe, T., Ishii, G., Kojima, M., Kinoshitá, T., Ueno, T., Esumi, H., & Ochiai, A. (2008) · Cancer Science · doi:10.1111/j.1349-7006.2008.00893.x · Cited by 279 · see citing works
Cancer Cell MetabolismPreprint
Cairns, R. A., Harris, I. S., McCracken, S. A., & Mak, T. W. (2011) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2011.76.012856 · Cited by 223 · see citing works
Elevated serum interleukin-6 levels in patients with pancreatic cancer.
Okada, S., Okusaka, T., Ishii, H., Kyogoku, A., Yoshimori, M., Kajimura, N., Yamaguchi, K., & Kakizoe, T. (1998) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/28.1.12 · Cited by 150 · see citing works
Autophagy is essential to suppress cell stress and to allow BCR-Abl-mediated leukemogenesis
Altman, B. J., Jacobs, S., Mason, E. F., Michalek, R. D., Macintyre, A. N., Coloff, J. L., Ilkayeva, O., Jia, W. P., He, Y.-W., & Rathmell, J. C. (2010) · Oncogene · doi:10.1038/onc.2010.561 · Cited by 135 · see citing works
Molecular classification of neoplasms of the pancreas
Hruban, R. H., & Adsay, V. N. (2009) · Human Pathology · doi:10.1016/j.humpath.2009.01.008 · Cited by 93 · see citing works
Kang, R., Tang, D., Livesey, K. M., Schapiro, N. E., Lotze, M. T., & Zeh, H. J. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3378 · Cited by 90 · see citing works
Self-citationApoptosis promotes early tumorigenesis
Tang, D., Lotze, M. T., Kang, R., & Zeh, H. J. (2010) · Oncogene · doi:10.1038/onc.2010.573 · Cited by 63 · see citing works
Self-citationKang, R., Tang, D., Loze, M. T., & Zeh, H. J. (2010) · Autophagy · doi:10.4161/auto.7.1.13852 · Cited by 44 · see citing works
Self-citationDiNorcia, J., Lee, M. K., Moroziewicz, D. N., Winner, M. D., Suman, P., Bao, F., Remotti, H. E., Zou, Y. S., Yan, S. F., Qiu, W., et al. (2011) · Journal of Gastrointestinal Surgery · doi:10.1007/s11605-011-1754-9 · Cited by 42 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
PAMP s and DAMP s: signal 0s that spur autophagy and immunity
Tang, D., Kang, R., Coyne, C. B., Zeh, H. J., & Lotze, M. T. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01146.x · Cited by 1,250 · see citing works
Self-citationKang, R., Chen, R., Zhang, Q., Hou, W., Wu, S., Cao, L., Huang, J., Yu, Y., Fan, X.-G., Yan, Z., et al. (2014) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2014.05.001 · Cited by 956 · see citing works
Self-citationIL-6 and related cytokines as the critical lynchpins between inflammation and cancer
Taniguchi, K., & Karin, M. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2014.01.001 · Cited by 713 · see citing works
Dai, E., Han, L., Liu, J., Xie, Y., Kroemer, G., Klionsky, D. J., Zeh, H. J., Kang, R., Wang, J., & Tang, D. (2020) · Autophagy · doi:10.1080/15548627.2020.1714209 · Cited by 613 · see citing works
Self-citationCellular signalling of the receptor for advanced glycation end products (RAGE)
Xie, J., Méndez, J. D., Méndez-Valenzuela, V., & Aguilar-Hernández, M. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.06.013 · Cited by 515 · see citing works
HMGB1 in Cancer: Good, Bad, or Both?
Kang, R., Zhang, Q., Zeh, H. J., Lotze, M. T., & Tang, D. (2013) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-0495 · Cited by 496 · see citing works
Self-citationMace, T. A., Ameen, Z., Collins, A., Wojcik, S. E., Mair, M., Young, G. S., Fuchs, J. R., Eubank, T. D., Frankel, W. L., Bekaii‐Saab, T., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-4601 · Cited by 413 · see citing works
Rungratanawanich, W., Qu, Y., Wang, X., Essa, M. M., & Song, B.-J. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00561-7 · Cited by 411 · see citing works
New insights into pancreatic cancer-induced paraneoplastic diabetes
Sah, R. P., Nagpal, S. J. S., Mukhopadhyay, D., & Chari, S. T. (2013) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2013.49 · Cited by 336 · see citing works
Regulation of autophagy by stress-responsive transcription factors
Pietrocola, F., Izzo, V., Niso‐Santano, M., Vacchelli, E., Galluzzi, L., Maiuri, M. C., & Kroemer, G. (2013) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2013.05.008 · Cited by 270 · see citing works
Boone, B. A., Bahary, N., Zureikat, A. H., Moser, A. J., Normolle, D. P., Wu, W.-C., Singhi, A. D., Bao, P., Bartlett, D. L., Liotta, L. A., et al. (2015) · Annals of Surgical Oncology · doi:10.1245/s10434-015-4566-4 · Cited by 234 · see citing works
Self-citationAutophagy-dependent secretion: mechanism, factors secreted, and disease implications
New, J., & Thomas, S. M. (2019) · Autophagy · doi:10.1080/15548627.2019.1596479 · Cited by 226 · see citing works
Kang, R., Tang, D., Schapiro, N. E., Loux, T., Livesey, K. M., Billiar, T. R., Wang, H., Houten, B. V., Lotze, M. T., & Zeh, H. J. (2013) · Oncogene · doi:10.1038/onc.2012.631 · Cited by 230 · see citing works
Self-citationThe immune network in pancreatic cancer development and progression
Wörmann, S. M., Diakopoulos, K. N., Lesina, M., & Algül, H. (2013) · Oncogene · doi:10.1038/onc.2013.257 · Cited by 202 · see citing works
Strange attractors: DAMPs and autophagy link tumor cell death and immunity
Hou, W., Zhang, Q., Yan, Z., Chen, R., Zeh, H. J., Kang, R., Lotze, M. T., & Tang, D. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.493 · Cited by 194 · see citing works
Self-citationInflammatory signaling cascades and autophagy in cancer
Monkkonen, T., & Debnath, J. (2017) · Autophagy · doi:10.1080/15548627.2017.1345412 · Cited by 188 · see citing works
Maycotte, P., Gearheart, C. M., Barnard, R., Aryal, S., Levy, J. M. M., Fosmire, S. P., Hansen, R. J., Morgan, M. J., Porter, C. C., Gustafson, D. L., et al. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-3470 · Cited by 185 · see citing works
Kabacaoğlu, D., Ciecielski, K. J., Ruess, D. A., & Algül, H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01878 · Cited by 175 · see citing works
Lycorine: A prospective natural lead for anticancer drug discovery
Roy, M., Liang, L., Xiao, X., Feng, P., Ye, M., & Liu, J. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.07.147 · Cited by 164 · see citing works
Regulation and function of autophagy in pancreatic cancer
Li, J., Chen, X., Kang, R., Zeh, H. J., Klionsky, D. J., & Tang, D. (2020) · Autophagy · doi:10.1080/15548627.2020.1847462 · Cited by 160 · see citing works
Self-citationLan, C.-Y., Chen, S.-Y., Kuo, C., Lu, C., & Yen, G. (2019) · Journal of Food and Drug Analysis · doi:10.1016/j.jfda.2019.07.001 · Cited by 159 · see citing works
Eat-Me: Autophagy, Phagocytosis, and Reactive Oxygen Species Signaling
Vernon, P. J., & Tang, D. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4810 · Cited by 156 · see citing works
Self-citationSTAT3 in cancer: A double edged sword
Avalle, L., Camporeale, A., Camperi, A., & Poli, V. (2017) · Cytokine · doi:10.1016/j.cyto.2017.03.018 · Cited by 156 · see citing works
Nasser, M. W., Wani, N. A., Ahirwar, D. K., Powell, C. A., Ravi, J., Elbaz, M., Zhao, H., Padilla, L., Zhang, X., Shilo, K., et al. (2015) · Cancer Research · doi:10.1158/0008-5472.can-14-2161 · Cited by 151 · see citing works
Methylglyoxal and Its Adducts: Induction, Repair, and Association with Disease
Lai, S. W. T., Gonzalez, E. D. J. L., Zoukari, T., Ki, P., & Shuck, S. C. (2022) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.2c00160 · Cited by 154 · see citing works
Mitochondrial Stat3, the need for design thinking
Yang, R., & Rincon, M. (2016) · International Journal of Biological Sciences · doi:10.7150/ijbs.15153 · Cited by 147 · see citing works
Interleukin-6 in inflammatory and malignant diseases of the pancreas
Lesina, M., Wörmann, S. M., Neuhöfer, P., Song, L., & Algül, H. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2014.01.002 · Cited by 146 · see citing works
DAMPs, ageing, and cancer: The ‘DAMP Hypothesis’
Huang, J., Xie, Y., Sun, X., Zeh, H. J., Kang, R., Lotze, M. T., & Tang, D. (2015) · Ageing Research Reviews · doi:10.1016/j.arr.2014.10.004 · Cited by 144 · see citing works
Self-citationIntracellular HMGB1 as a novel tumor suppressor of pancreatic cancer
Kang, R., Xie, Y., Zhang, Q., Hou, W., Jiang, Q., Zhu, S., Liu, J., Zeng, D., Wang, H., Bartlett, D. L., et al. (2017) · Cell Research · doi:10.1038/cr.2017.51 · Cited by 136 · see citing works
Self-citationRole of advanced glycation end products in carcinogenesis and their therapeutic implications
Schröter, D., & Höhn, A. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190130145549 · Cited by 126 · see citing works
Targeting of RAGE-ligand signaling impairs breast cancer cell invasion and metastasis
Kwak, T., Drews‐Elger, K., Ergonul, A. B., Miller, P. C., Braley, A. E., Hwang, G. H., Zhao, D., Besser, A., Yamamoto, Y., Yamamoto, H., et al. (2016) · Oncogene · doi:10.1038/onc.2016.324 · Cited by 130 · see citing works
Extracellular HMGB1 promotes differentiation of nurse-like cells in chronic lymphocytic leukemia
Jia, L., Clear, A. J., Liu, F., Matthews, J., Uddin, N., McCarthy, A., Hoxha, E., Durance, C., Iqbal, S., & Gribben, J. G. (2014) · Blood · doi:10.1182/blood-2013-10-529610 · Cited by 115 · see citing works
Porporato, P. E., Payen, V. L., Baselet, B., & Sonveaux, P. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2100-2 · Cited by 110 · see citing works
Interleukin-6: a villain in the drama of pancreatic cancer development and progression
Holmer, R., Goumas, F. A., Waetzig, G. H., Rose‐John, S., & Kalthoff, H. (2014) · Hepatobiliary & pancreatic diseases international · doi:10.1016/s1499-3872(14)60259-9 · Cited by 108 · see citing works
IL-6 Inhibits Starvation-induced Autophagy via the STAT3/Bcl-2 Signaling Pathway
Qin, B., Zhou, Z. L., He, J., Yan, C., & Ding, S. (2015) · Scientific Reports · doi:10.1038/srep15701 · Cited by 95 · see citing works
Glycation changes molecular organization and charge distribution in type I collagen fibrils
Bansode, S. B., Bashtanova, U., Li, R., Clark, J. P., Müller, K. H., Puszkarska, A. M., Goldberga, I., Chetwood, H. H., Reid, D. G., Colwell, L. J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-60250-9 · Cited by 95 · see citing works
RAGE is essential for oncogenic KRAS-mediated hypoxic signaling in pancreatic cancer
Kang, R., Hou, W., Zhang, Q., Chen, R., Lee, Y. J., Bartlett, D. L., Lotze, M. T., Tang, D., & Zeh, H. J. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.445 · Cited by 93 · see citing works
Self-citationMyeloid-Derived Suppressor Cells and Pancreatic Cancer: Implications in Novel Therapeutic Approaches
Thyagarajan‐Sahu, A., Alshehri, M. S. A., Miller, K. L., Sherwin, C. M. T., Travers, J. B., & Sahu, R. P. (2019) · Cancers · doi:10.3390/cancers11111627 · Cited by 90 · see citing works
You eat what you are: autophagy inhibition as a therapeutic strategy in leukemia
Sehgal, A. R., Koenig, H., Johnson, D. E., Tang, D., Amaravadi, R. K., Boyiadzis, M. M., & Lotze, M. T. (2014) · Leukemia · doi:10.1038/leu.2014.349 · Cited by 88 · see citing works
Self-citationMalik, P., Chaudhry, N., Mittal, R., & Mukherjee, T. K. (2015) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2015.05.020 · Cited by 88 · see citing works
STAT3 and Its Targeting Inhibitors in Oral Squamous Cell Carcinoma
Jiang, M., & Li, B. (2022) · Cells · doi:10.3390/cells11193131 · Cited by 78 · see citing works
Autophagy Inhibition by Sustained Overproduction of IL6 Contributes to Arsenic Carcinogenesis
Qi, Y., Zhang, M., Li, H., Frank, J. A., Dai, L., Liu, H., Zhang, Z., Wang, C., & Chen, G. (2014) · Cancer Research · doi:10.1158/0008-5472.can-13-3182 · Cited by 77 · see citing works
Diabetes and Pancreatic Cancer—A Dangerous Liaison Relying on Carbonyl Stress
Menini, S., Iacobini, C., Vitale, M., Pesce, C. M., & Pugliese, G. (2021) · Cancers · doi:10.3390/cancers13020313 · Cited by 75 · see citing works
Nucleus, mitochondrion, or reticulum? STAT3 à La Carte
Avalle, L., & Poli, V. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19092820 · Cited by 74 · see citing works
Role of Receptor for Advanced Glycation End Products (RAGE) and Its Ligands in Cancer Risk
Yamagishi, S., Matsui, T., & Fukami, K. (2014) · Rejuvenation Research · doi:10.1089/rej.2014.1625 · Cited by 71 · see citing works
Autophagy and Transporter-Based Multi-Drug Resistance
Kumar, P., Zhang, D., Degenhardt, K., & Chen, Z. (2012) · Cells · doi:10.3390/cells1030558 · Cited by 70 · see citing works
Chen, Y., Li, X., Lin, X., Liang, H., Liu, X., Zhang, X., Zhang, Q., Zhou, F., Chen, Y., Lei, L., et al. (2022) · Thrombosis Journal · doi:10.1186/s12959-022-00384-0 · Cited by 65 · see citing works
Hypoxia driven glycation: Mechanisms and therapeutic opportunities
Khan, M. I., Rath, S., Adhami, V. M., & Mukhtar, H. (2017) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2017.05.008 · Cited by 64 · see citing works
Perspectives Regarding the Intersections between STAT3 and Oxidative Metabolism in Cancer
Chun, K., Jang, J., & Kim, D. (2020) · Cells · doi:10.3390/cells9102202 · Cited by 62 · see citing works
The ACSL4 Network Regulates Cell Death and Autophagy in Diseases
Chen, F., Kang, R., Liu, J., & Tang, D. (2023) · Biology · doi:10.3390/biology12060864 · Cited by 63 · see citing works
Self-citationSTAT3 down regulates LC3 to inhibit autophagy and pancreatic cancer cell growth
Gong, J., Muñoz, A. R., Chan, D. C. F., Ghosh, R., & Kumar, A. P. (2014) · Oncotarget · doi:10.18632/oncotarget.1810 · Cited by 63 · see citing works
Kang, R., Chen, R., Xie, M., Cao, L., Lotze, M. T., Tang, D., & Zeh, H. J. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502340 · Cited by 62 · see citing works
Self-citationThe Interaction Between Autophagy and JAK/STAT3 Signaling Pathway in Tumors
Xu, J., Zhang, J., Mao, Q., Wu, J., & Wang, Y. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.880359 · Cited by 60 · see citing works
Autophagy in pancreatic cancer pathogenesis and treatment.
Kang, R., & Tang, D. (2012) · Europe PMC (PubMed Central) · Cited by 60 · see citing works
Self-citationMenini, S., Iacobini, C., de Latouliere, L., Manni, I., Ionta, V., Fantauzzi, C. B., Pesce, C. M., Cappello, P., Novelli, F., Piaggio, G., et al. (2018) · The Journal of Pathology · doi:10.1002/path.5072 · Cited by 58 · see citing works
Silveira, É. A., Filho, R. R. D. S., Spexoto, M. C. B., Haghighatdoost, F., Sarrafzadegan, N., & de Oliveira, C. M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094339 · Cited by 56 · see citing works
Alternative Splicing of the RAGE Cytoplasmic Domain Regulates Cell Signaling and Function
Jules, J., Maiguel, D. A., & Hudson, B. I. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078267 · Cited by 57 · see citing works
Chen, C., Abell, A. M., Moon, Y. S., & Kim, K. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.399790 · Cited by 59 · see citing works
Vernon, P. J., Loux, T., Schapiro, N. E., Kang, R., Muthuswamy, R., Kaliński, P., Tang, D., Lotze, M. T., & Zeh, H. J. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201151 · Cited by 57 · see citing works
Self-citationPanIN-specific regulation of Wnt signaling by HIF2α during early pancreatic tumorigenesis
Criscimanna, A., Duan, L.-J., Rhodes, J., Fendrich, V., Wickline, E., Hartman, D., Monga, S., Lotze, M., Gittes, G., Fong, G., et al. (2013) · Cancer Research · doi:10.1158/0008-5472.can-13-0566 · Cited by 51 · see citing works
Self-citationThe interactive role of inflammatory mediators and metabolic reprogramming in pancreatic cancer
Ohara, Y., Valenzuela, P., & Hussain, S. P. (2022) · Trends in cancer · doi:10.1016/j.trecan.2022.03.004 · Cited by 53 · see citing works
Ménage à Trois in stress: DAMPs, redox and autophagy
Li, G., Tang, D., & Lotze, M. T. (2013) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2013.08.002 · Cited by 55 · see citing works
Self-citationPortillo, J. C., Muniz-Feliciano, L., Corcino, Y. L., Lee, S. J., Grol, J. V., Parsons, S. J., Schiemann, W. P., & Subauste, C. S. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006671 · Cited by 54 · see citing works
Hashimoto, S., Hashimoto, A., Muromoto, R., Kitai, Y., Oritani, K., & Matsuda, T. (2022) · Cells · doi:10.3390/cells11162618 · Cited by 50 · see citing works
Palanissami, G., & Paul, S. F. D. (2023) · Exploration of Targeted Anti-tumor Therapy · doi:10.37349/etat.2023.00170 · Cited by 51 · see citing works
Xu, X., Zhi, T., Chao, H., Jiang, K., Liu, Y., Bao, Z., Fan, L., Wang, D., Li, Z., Liu, N., et al. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.02.011 · Cited by 51 · see citing works
Pancreatic cancer and diabetes: A two-way relationship in the perspective of diabetologist
Salvatore, T., Marfella, R., Rizzo, M. R., & Sasso, F. C. (2015) · International Journal of Surgery · doi:10.1016/j.ijsu.2015.06.063 · Cited by 50 · see citing works
Lin, Q., Fan, C., Gomez‐Arroyo, J. G., Raemdonck, K. V., Meuchel, L. W., SKINNER, J. T., Everett, A. D., Fang, X., MacDonald, A. A., Yamaji-Kegan, K., et al. (2019) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.119.312907 · Cited by 50 · see citing works
Snyder‐Talkington, B. N., Dong, C., Sargent, L. M., Porter, D. W., Staska, L. M., Hubbs, A. F., Raese, R. A., McKinney, W., Chen, B. T., Battelli, L. A., et al. (2015) · Journal of Applied Toxicology · doi:10.1002/jat.3157 · Cited by 48 · see citing works
Udaya Rajesh, R., & Sangeetha, D. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155902 · Cited by 45 · see citing works
Sakaguchi, M., Murata, H., Aoyama, Y., Hibino, T., Putranto, E. W., Ruma, I. M. W., Inoue, Y., Sakaguchi, Y. M., Yamamoto, K.-I., Kinoshita, R., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.573071 · Cited by 45 · see citing works
Knockdown of RAGE inhibits growth and invasion of gastric cancer cells
Xu, X. C., Abuduhadeer, X., Zhang, W., Li, T., Gao, H., & Wang, Y. H. (2013) · European Journal of Histochemistry · doi:10.4081/ejh.2013.e36 · Cited by 45 · see citing works
Chang, H.-H., & Eibl, G. (2019) · Cells · doi:10.3390/cells8070673 · Cited by 47 · see citing works
Braley, A. E., Kwak, T., Jules, J., Harja, E., Landgraf, R., & Hudson, B. I. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.702399 · Cited by 43 · see citing works
Larrue, C., Heydt, Q., Saland, E., Boutzen, H., Kaoma, T., Sarry, J., Joffre, C., & Récher, C. (2019) · Oncogenesis · doi:10.1038/s41389-019-0148-9 · Cited by 43 · see citing works
Leveling Up the Controversial Role of Neutrophils in Cancer: When the Complexity Becomes Entangled
Sionov, R. V. (2021) · Cells · doi:10.3390/cells10092486 · Cited by 42 · see citing works
Cross, K., Vetter, S. W., Alam, Y., Hasan, M. Z., Nath, A. D., & Leclerc, E. (2024) · Biomolecules · doi:10.3390/biom14121550 · Cited by 43 · see citing works
Haque, E., Kamil, M., Hasan, A., Irfan, S., Sheikh, S., Khatoon, A., Nazir, A., & Mir, S. S. (2019) · Glycobiology · doi:10.1093/glycob/cwz073 · Cited by 41 · see citing works
The Redox Protein High-Mobility Group Box 1 in Cell Death and Cancer
Chen, R., Zou, J., Kang, R., & Tang, D. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0236 · Cited by 38 · see citing works
Self-citationRelaxin alleviates TGFβ1-induced cardiac fibrosis via inhibition of Stat3-dependent autophagy
Yuan, Y., Zhang, Y., Han, X., Li, Y., Zhao, X., Sheng, L., & Li, Y. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.09.110 · Cited by 35 · see citing works
Diminished levels of the soluble form of RAGE are related to poor survival in malignant melanoma
Wagner, N. B., Weide, B., Reith, M., Tarnanidis, K., Kehrel, C., Lichtenberger, R., Pflugfelder, A., Herpel, E., Eubel, J., Ikenberg, K., et al. (2015) · International Journal of Cancer · doi:10.1002/ijc.29619 · Cited by 34 · see citing works
Li, C., Liu, Y., Liu, C., Chen, F., Xie, Y., Zeh, H. J., Yu, C., Liu, J., Tang, D., & Kang, R. (2025) · Science Translational Medicine · doi:10.1126/scitranslmed.adp4986 · Cited by 36 · see citing works
Self-citationRAGE-dependent potentiation of TRPV1 currents in sensory neurons exposed to high glucose
Lam, D., Momeni, Z., Theaker, M., Jagadeeshan, S., Yamamoto, Y., Ianowski, J. P., & Campanucci, V. A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193312 · Cited by 32 · see citing works
RAGE overexpression confers a metastatic phenotype to the WM115 human primary melanoma cell line
Meghnani, V., Vetter, S. W., & Leclerc, E. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.02.013 · Cited by 31 · see citing works
Dicarbonyl/l-xylulose reductase (DCXR): The multifunctional pentosuria enzyme
Lee, S.-K., Le, T. S., Choi, H., & Ahnn, J. (2013) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2013.08.010 · Cited by 30 · see citing works
Tang, S., Bonaroti, J. W., Unlu, S., Liang, X., Tang, D., Zeh, H. J., & Lotze, M. T. (2013) · Pancreas · doi:10.1097/mpa.0b013e3182854ab0 · Cited by 30 · see citing works
Self-citationInvestigation of phosphoproteome in RAGE signaling
Batkulwar, K., Bansode, S. B., Patil, G. V., Godbole, R. K., Kazi, R. S., Chinnathambi, S., Shanmugam, D., & Kulkarni, M. J. (2014) · PROTEOMICS · doi:10.1002/pmic.201400169 · Cited by 30 · see citing works
Resistance Training Attenuates Activation of STAT3 and Muscle Atrophy in Tumor-Bearing Mice
Testa, M. T. D. J., Cella, P. S., Marinello, P. C., Frajacomo, F., Padilha, C. D. S., Perandini, P. C., Moura, F., Duarte, J., Cecchini, R., Guarnier, F., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.880787 · Cited by 26 · see citing works
Mir, A. R., Uddin, M., Khan, F. I., Alam, K., & Ali, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136197 · Cited by 28 · see citing works
RAGE maintains high levels of NFκB and oncogenic Kras activity in pancreatic cancer
Azizan, N., Suter, M., Liu, Y., & Logsdon, C. D. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.08.147 · Cited by 27 · see citing works
Hypoxia and the Receptor for Advanced Glycation End Products (RAGE) Signaling in Cancer
Taneja, S., Vetter, S. W., & Leclerc, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158153 · Cited by 27 · see citing works
Chen, R.-J., Lyu, Y.-J., Chen, Y., Lee, Y.-C., Pan, M., Ho, Y., & Wang, Y. (2021) · Molecules · doi:10.3390/molecules26216741 · Cited by 27 · see citing works
HMGB1 in Hormone-Related Cancer: a Potential Therapeutic Target
Srinivasan, M., Banerjee, S., Palmer, A., Zheng, G., Chen, A., Bosland, M. C., Kajdacsy‐Balla, A., Kalyanasundaram, R., & Munirathinam, G. (2014) · Hormones and Cancer · doi:10.1007/s12672-014-0175-0 · Cited by 27 · see citing works
RAGE Up-Regulation Differently Affects Cell Proliferation and Migration in Pancreatic Cancer Cells
Swami, P., Thiyagarajan, S., Vidger, A. J., Indurthi, V. S. K., Vetter, S. W., & Leclerc, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21207723 · Cited by 26 · see citing works
Chen, S., Hsu, Y., Wang, S., Chen, Y., Hong, C., & Yen, G. (2022) · Phytotherapy Research · doi:10.1002/ptr.7385 · Cited by 25 · see citing works
Healey, G. D., Pan‐Castillo, B., García-Parra, J., Davies, J., Roberts, S., Jones, E., Dhar, K. K., Nandanan, S., Tofazzal, N., Piggott, L., et al. (2019) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-019-0765-z · Cited by 25 · see citing works
Hu, Z., Fang, W., Liu, Y., Liang, H., Chen, W., & Wang, H. (2021) · Molecular Medicine Reports · doi:10.3892/mmr.2021.11969 · Cited by 23 · see citing works
Targeting secretory autophagy in solid cancers: mechanisms, immune regulation and clinical insights
Li, X., & Zhao, H. (2025) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00603-0 · Cited by 23 · see citing works
Mitophagy in Pancreatic Cancer
Xie, Y., Liu, J., Kang, R., & Tang, D. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.616079 · Cited by 22 · see citing works
Self-citationThe Multifaceted Effects of Autophagy on the Tumor Microenvironment
Kang, R., Zeh, H. J., Lotze, M. T., & Tang, D. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-35727-6_7 · Cited by 22 · see citing works
Self-citation
- Authors
- Kang, R., Loux, T., Tang, D., Schapiro, N. E., Vernon, P., Livesey, K. M., Krasinskas, A., Lotze, M. T., & Zeh, H. J.
- Affiliations
- UPMC Hillman Cancer Center (US)
- University of Pittsburgh Medical Center (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-04-16
- Volume
- 109
- Issue
- 18
- Pages
- 7031-7036
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3345001
- OpenAlex
- W2017280299
- Cited by
- 163
- References
- 34
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 7 · 2023: 8 · 2022: 10 · 2021: 14 · 2020: 11 · 2019: 14 · 2018: 13 · 2017: 8 · 2016: 10 · 2015: 12 · 2014: 17 · 2013: 18 · 2012: 8
- FWCI
- 11.28
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (UL1TR000005)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- receptor for advanced glycation end products, RAGE, pancreatic carcinogenesis, pancreatic neoplasia, autophagy, STAT3 signaling, interleukin-6, mitochondrial signaling, KRAS G12D, Pdx1-Cre, ATP production
- MeSH terms
- Receptor for Advanced Glycation End Products, Adenosine Triphosphate, Animals, Autophagy, Humans, Mice, Inbred C57BL, Mice, Mutant Strains, Mice, Transgenic, Mitochondria, Pancreatic Neoplasms, Phosphorylation, Receptors, Immunologic, Signal Transduction, Interleukin-6, Proto-Oncogene Proteins p21(ras), Cell Line, Tumor, STAT3 Transcription Factor, Mice, Mice, 129 Strain, Tumor Microenvironment
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review