The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
Cancer-Secreted miR-105 Destroys Vascular Endothelial Barriers to Promote Metastasis
Open accessAbstract
Cancer-secreted microRNAs (miRNAs) are emerging mediators of cancer-host crosstalk. Here we show that miR-105, which is characteristically expressed and secreted by metastatic breast cancer cells, is a potent regulator of migration through targeting the tight junction protein ZO-1. In endothelial monolayers, exosome-mediated transfer of cancer-secreted miR-105 efficiently destroys tight junctions and the integrity of these natural barriers against metastasis. Overexpression of miR-105 in nonmetastatic cancer cells induces metastasis and vascular permeability in distant organs, whereas inhibition of miR-105 in highly metastatic tumors alleviates these effects. miR-105 can be detected in the circulation at the premetastatic stage, and its levels in the blood and tumor are associated with ZO-1 expression and metastatic progression in early-stage breast cancer.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“Many studies have also demonstrated that extracellular miRNAs can exert biological functions in recipient cells to regulate their activity, thereby acting as intercellular signaling molecules.”
From Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation (2018) · cites this paper as [134]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
RETRACTED: MicroRNA signatures of tumor-derived exosomes as diagnostic biomarkers of ovarian cancer
Taylor, D. D., & Gerçel-Taylor, Ç. (2008) · Gynecologic Oncology · doi:10.1016/j.ygyno.2008.04.033 · Cited by 2,333
RetractedValadi, H., Ekström, K., Bossios, A., Sjöstrand, M., Lee, J. J., & Lötvall, J. O. (2007) · Nature Cell Biology · doi:10.1038/ncb1596 · Cited by 12,834
Circulating microRNAs as stable blood-based markers for cancer detection
Mitchell, P. S., Parkin, R. K., Kroh, E. M., Fritz, B. R., Wyman, S. K., Pogosova-Agadjanyan, E. L., Peterson, A., Noteboom, J., O'Briant, K. C., Allen, A., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804549105 · Cited by 7,969
MicroRNA signatures in human cancers
Calin, G. A., & Croce, C. M. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1997 · Cited by 7,668
Isolation and Characterization of Exosomes from Cell Culture Supernatants and Biological Fluids
Théry, C., Amigorena, S., Raposo, G., & Clayton, A. (2006) · Current Protocols in Cell Biology · doi:10.1002/0471143030.cb0322s30 · Cited by 5,766
Exosomes: composition, biogenesis and function
Théry, C., Zitvogel, L., & Amigorena, S. (2002) · Nature reviews. Immunology · doi:10.1038/nri855 · Cited by 5,478
The distribution of secondary growths in cancer of the breast.
Paget, S. (1889) · The Lancet · doi:10.1016/s0140-6736(00)49915-0 · Cited by 5,277
Skog, J., Würdinger, T., van Rijn, S., Meijer, D. H., Gainche, L., Curry, W. T., Carter, B. S., Krichevsky, A. M., & Breakefield, X. O. (2008) · Nature Cell Biology · doi:10.1038/ncb1800 · Cited by 5,001
MicroRNA Gene Expression Deregulation in Human Breast Cancer
Iorio, M. V., Ferracin, M., Liu, C.-G., Veronese, A., Spizzo, R., Sabbioni, S., Magri, E., Pedriali, M., Fabbri, M., Campiglio, M., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1783 · Cited by 4,053
Dissemination and growth of cancer cells in metastatic sites
Chambers, A. F., Groom, A. C., & MacDonald, I. C. (2002) · Nature reviews. Cancer · doi:10.1038/nrc865 · Cited by 4,018
Cited by
Sorted by citations
Items 501–600 of 1,001
Stefańska, K., Józkowiak, M., Volponi, A. A., Shibli, J. A., Golkar‐Narenji, A., Antosik, P., Bukowska, D., Piotrowska‐Kempisty, H., Mozdziak, P. E., Dzięgiel, P., et al. (2023) · Cells · doi:10.3390/cells12030356 · Cited by 56
MicroRNAs in cancer metastasis: biological and therapeutic implications
Sell, M. C., Ramlogan‐Steel, C. A., Steel, J. C., & Dhungel, B. P. (2023) · Expert Reviews in Molecular Medicine · doi:10.1017/erm.2023.7 · Cited by 53
“40), e.g. miR-105 regulates the metastasis of breast cancer by inhibiting ZO-1 (Ref.”
MiR‐605 represses PSMD10/Gankyrin and inhibits intrahepatic cholangiocarcinoma cell progression
Li, J., Tian, F., Li, D., Chen, J., Jiang, P., Zheng, S., Li, X., & Wang, S. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.08.008 · Cited by 53
Noncoding RNAs in breast cancer
Lo, P., Wolfson, B., Zhou, X., Duru, N., Gernapudi, R., & Zhou, Q. Y. (2015) · Briefings in Functional Genomics · doi:10.1093/bfgp/elv055 · Cited by 54
MicroRNA Theranostics in Prostate Cancer Precision Medicine
Matin, F., Jeet, V., Clements, J. A., Yousef, G. M., & Batra, J. (2016) · Clinical Chemistry · doi:10.1373/clinchem.2015.242800 · Cited by 53
Promising therapeutic role of miR-27b in tumor
Ding, L., Ni, J., Yang, F., Huang, L., Deng, H., Wu, Y. F., Ding, X., & Tang, J. (2017) · Tumor Biology · doi:10.1177/1010428317691657 · Cited by 54
Emerging ways to treat breast cancer: will promises be met?
Samadi, P., Saki, S., Dermani, F. K., Pourjafar, M., & Saidijam, M. (2018) · Cellular Oncology · doi:10.1007/s13402-018-0409-1 · Cited by 54
Exosome-Derived ADAM17 Promotes Liver Metastasis in Colorectal Cancer
Sun, J., Lu, Z., Fu, W., Lu, K., Gu, X., Xu, F., Dai, J., Yang, Y., & Jiang, J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.734351 · Cited by 54
Sabir, F., Qindeel, M., Zeeshan, M., Ain, Q. U., Rahdar, A., Barani, M., González, E., & Aboudzadeh, M. A. (2021) · Processes · doi:10.3390/pr9040621 · Cited by 56
Chemokines orchestrate tumor cells and the microenvironment to achieve metastatic heterogeneity
Saxena, S., & Singh, R. K. (2021) · Cancer and Metastasis Reviews · doi:10.1007/s10555-021-09970-6 · Cited by 54
Exosomes: a potential diagnostic and treatment modality in the quest for counteracting cancer
Patel, G., Agnihotri, T. G., Gitte, M., Shinde, T., Gomte, S. S., Goswami, R., & Jain, A. (2023) · Cellular Oncology · doi:10.1007/s13402-023-00810-z · Cited by 53
Tumor-derived nanoseeds condition the soil for metastatic organotropism
Hu, M., Kenific, C. M., Boudreau, N. J., & Lyden, D. C. (2023) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2023.05.003 · Cited by 53
Breast cancer cell-secreted miR-199b-5p hijacks neurometabolic coupling to promote brain metastasis
Ruan, X., Yan, W., Cao, M., Daza, R. A. M., Fong, M., Yang, K., Wu, J., Liu, X., Palomares, M. R., Wu, X., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48740-0 · Cited by 55
Alsibai, K. D., & Meseure, D. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24548 · Cited by 53
Exosomes as emerging players in cancer biology
Couto, N., Caja, S., Maia, J., Moraes, M. C. S., & Costa‐Silva, B. (2018) · Biochimie · doi:10.1016/j.biochi.2018.03.006 · Cited by 52
Exosomes in cancer: Small transporters with big functions
Li, X., Wang, Y., Wang, Q., Liu, Y., Bao, W., & Wu, S. (2018) · Cancer Letters · doi:10.1016/j.canlet.2018.07.037 · Cited by 51
Integrin Regulation in Immunological and Cancerous Cells and Exosomes
Soe, Z. Y., Park, E. J., & Shimaoka, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22042193 · Cited by 52
MicroRNAs in Cancer: From Gene Expression Regulation to the Metastatic Niche Reprogramming
Semina, E. V., Rysenkova, K. D., Troyanovskiy, K. E., Shmakova, A., & Rubina, K. A. (2021) · Biochemistry (Moscow) · doi:10.1134/s0006297921070014 · Cited by 50
Cancer-induced systemic pre-conditioning of distant organs: building a niche for metastatic cells
Rabas, N., Ferreira, R. M. M., Blasio, S. D., & Malanchi, I. (2024) · Nature reviews. Cancer · doi:10.1038/s41568-024-00752-0 · Cited by 58
“Mechanistically, these range from direct silencing of junctional components in the case of miRNA-containing EV transfer 67–69 , to enzymatic products in EVs driving purinergic signalling in endothelial cells, resulting in loss of junctional β-catenin, vascular destabilization and metastasis 70 .”
Functional role of extracellular vesicles and lipoproteins in the tumour microenvironment
Menard, J. A., Cerezo-Magaña, M., & Belting, M. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0480 · Cited by 50
Fan, K., Spassova, I., Gravemeyer, J., Ritter, C., Horny, K., Lange, A., Gambichler, T., Ødum, N., Schrama, D., Schadendorf, D., et al. (2020) · Oncogene · doi:10.1038/s41388-020-01576-6 · Cited by 51
Cosentino, G., Plantamura, I., Tagliabue, E., Iorio, M. V., & Cataldo, A. (2021) · Cancers · doi:10.3390/cancers13153691 · Cited by 52
Brena, D., Huang, M., & Bond, V. C. (2021) · Translational Oncology · doi:10.1016/j.tranon.2021.101286 · Cited by 51
Emerging Role of Extracellular Vesicles and Cellular Communication in Metastasis
Forder, A., Hsing, C.-Y., Trejo, J., & Garnis, C. (2021) · Cells · doi:10.3390/cells10123429 · Cited by 53
Molecular functions and therapeutic applications of exosomal noncoding RNAs in cancer
Liu, Q., He, Y., & Xu, W. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00744-w · Cited by 50
Exosomal non-coding RNAs: a promising cancer biomarker
Yang, H., Fu, H., Xu, W., & Zhang, X. (2016) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2016-0029 · Cited by 50
“Exosomes from metastatic breast cancer cells transfer miR-105 to degrade ZO-1 protein, leading to the destruction of tight junctions between endothelial cells and inducing the dissemination of tumor cells [11].”
BackgroundCancer cells exploit an orphan RNA to drive metastatic progression
Fish, L., Zhang, S., Yu, J. X., Culbertson, B., Zhou, A. Y., Goga, A., & Goodarzi, H. (2018) · Nature Medicine · doi:10.1038/s41591-018-0230-4 · Cited by 50
Stem cells and extracellular vesicles: biological regulators of physiology and disease
Borgovan, T., Crawford, L. A., Nwizu, C. C., & Quesenberry, P. J. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00017.2019 · Cited by 50
y Cajal, S. R., Segura, M. F., & Hümmer, S. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00281 · Cited by 50
Dengue haemorrhagic fever: a job done via exosomes?
Mishra, R., Lata, S., Ali, A., & Banerjea, A. C. (2019) · Emerging Microbes & Infections · doi:10.1080/22221751.2019.1685913 · Cited by 52
“…of recently recognized role of exosomes in transferring important biological materials (micro-RNA/transcription factors/cytokines/chemokines) in various diseases [47 – 49], it is logical to assume that these microvesicles could be instrumental in ful fi lling viral needs of spread and pathogenesis.”
BackgroundChen, J., Fei, X., Wang, J., & Cai, Z. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105041 · Cited by 52
Tumor-Derived Exosomes Modulate Primary Site Tumor Metastasis
Bai, S., Wang, Z., Wang, M., Li, J., Wei, Y., Xu, R., & Du, J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.752818 · Cited by 53
Song, J.-W., Zhu, J., Wu, X.-X., Tu, T., Huang, J.-Q., Chen, G.-Z., Liang, L.-Y., Zhou, C.-H., Xu, X., & Gong, L.-Y. (2021) · Cell Death & Disease · doi:10.1038/s41419-021-04265-8 · Cited by 51
Xuan, Z., Chen, C., Tang, W., Ye, S., Zheng, J., Zhao, Y., Shi, Z., Zhang, L., Sun, H., & Shao, C. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.689947 · Cited by 52
Dilsiz, N. (2021) · Future Science OA · doi:10.2144/fsoa-2021-0102 · Cited by 51
Exosomes participate in the carcinogenesis and the malignant behavior of gastric cancer
Yan, Y., Fu, G., Ye, Y., & Ming, L. (2017) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.2016.1278458 · Cited by 49
Ding, Y., Pan, Y., Liu, S., Jiang, F., & Jiao, J. (2017) · Cancer Biology & Therapy · doi:10.1080/15384047.2017.1323585 · Cited by 49
The distinct role of strand-specific miR-514b-3p and miR-514b-5p in colorectal cancer metastasis
Ren, L., Yan, T., Shen, C., Tang, J., Kong, X., Wang, Y., Chen, J., Liu, Q., He, J., Zhong, M., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0732-5 · Cited by 49
Cheng, W., Ma, J., Cao, P., Zhang, Y., Xu, C., Yi, Y., & Li, J. (2020) · Talanta · doi:10.1016/j.talanta.2020.121242 · Cited by 49
Mechanisms of Organ-Specific Metastasis of Breast CancerPreprint
Nolan, E., Kang, Y., & Malanchi, I. (2023) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a041326 · Cited by 52
Duan, S., Nordmeier, S., Byrnes, A. E., & Buxton, I. L. O. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020597 · Cited by 48
Emerging role of exosomes and exosomal microRNA in cancer: pathophysiology and clinical potential
Elewaily, M. I., & Elsergany, A. R. (2021) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-021-03534-5 · Cited by 48
Ye, Y., Wang, M., Wang, G., Mai, Z., Zhou, B., Han, Y., Zhuang, J., & Xia, W. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04741-8 · Cited by 48
Shan, Y., Li, X., You, B., Shi, S., Zhang, Q., & You, Y. (2015) · Oncology Reports · doi:10.3892/or.2015.4195 · Cited by 49
“Recent studies of microRNAs (miRNAs) suggest a potential role of these regulatory molecules as candidate oncogenes or tumor suppressors in cancer progression (3-5).”
Exosomes in Bone Sarcomas: Key Players in Metastasis
Chicón‐Bosch, M., & Tirado, Ò. M. (2020) · Cells · doi:10.3390/cells9010241 · Cited by 50
Visualizing cancer extravasation: from mechanistic studies to drug development
Cheng, X., & Cheng, K. (2020) · Cancer and Metastasis Reviews · doi:10.1007/s10555-020-09942-2 · Cited by 53
Asao, T., Tobias, G. C., Lucotti, S., Jones, D. R., Matei, I. R., & Lyden, D. C. (2023) · Extracellular Vesicles and Circulating Nucleic Acids · doi:10.20517/evcna.2023.37 · Cited by 51
“Nucleic acids packaged within EVPs, such as RNA, especially microRNAs, are another class of molecules that can be used as diagnostic and prognostic biomarkers for various types of cancer [27,52,61,85,86] , providing valuable information for cancer detection, diagnosis, prognosis, and monitoring.”
BackgroundInfluentialGandellini, P., Doldi, V., & Zaffaroni, N. (2017) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2017.03.005 · Cited by 48
Park, Y., & Kim, J. (2019) · BMB Reports · doi:10.5483/bmbrep.2019.52.3.308 · Cited by 47
Exosomal microRNAs-mediated intercellular communication and exosome-based cancer treatment
Shi, Z., Yang, X., Malichewe, C. V., Li, Y., & Guo, X. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.04.228 · Cited by 47
CD44 and Tumor-Derived Extracellular Vesicles (TEVs). Possible Gateway to Cancer Metastasis
Szatanek, R., & Baj-Krzyworzeka, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22031463 · Cited by 43
Lee, P.-J., Sui, Y.-H., Liu, T.-T., Tsang, N., Huang, C.-H., Lin, T.-Y., Chang, K., & Liu, S. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02456-5 · Cited by 47
Zhao, H., Ahirwar, D. K., Oghumu, S., Wilkie, T., Powell, C. A., Nasser, M. W., Satoskar, A. R., Li, D. Y., & Ganju, R. K. (2015) · Molecular Oncology · doi:10.1016/j.molonc.2015.10.007 · Cited by 46
miR-663a inhibits hepatocellular carcinoma cell proliferation and invasion by targeting HMGA2
Huang, W., Li, J., Guo, X., Zhao, Y., & Yuan, X. (2016) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2016.04.034 · Cited by 46
Exosome: a novel mediator in drug resistance of cancer cells.
Zhang, H.-D., Jiang, L.-H., Hou, J.-C., Zhong, S., Zhu, L.-P., Wang, D.-D., Zhou, S., Yang, S.-J., Wang, J., Zhang, Q., et al. (2018) · Epigenomics · doi:10.2217/epi-2017-0151 · Cited by 41
Morad, G., & Moses, M. A. (2019) · Journal of Extracellular Vesicles · doi:10.1080/20013078.2019.1627164 · Cited by 46
Cha, H., Hong, S., Park, J. H., & Park, H. H. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12121135 · Cited by 45
The Hallmarks of Cancer as Ecologically Driven Phenotypes
Somarelli, J. A. (2021) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2021.661583 · Cited by 46
Radiotherapy-induced tumor physical microenvironment remodeling to overcome immunotherapy resistance
Peng, J., Yin, X., Yun, W., Meng, X., & Huang, Z. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216108 · Cited by 46
Das, K., Paul, S., Ghosh, A., Gupta, S. K., Mukherjee, T., Shankar, P., Sharma, A., Keshava, S., Chauhan, S. C., Kashyap, V. K., et al. (2023) · Cancers · doi:10.3390/cancers15194879 · Cited by 47
“[127] Abbreviations: EGFR, extracellular growth factor receptor; AREG, amphiregulin; UCHL 1 , ubiquitin C–terminal hydrolase 1; TGF β , transforming growth factor beta; SMAD2, mothers against decapentaplegic homolog 2; PTX, paclitaxel; CD, cluster of differentiation; HOXD10, homeobox D10; KLF4,…”
BackgroundInfluentialExosomes in Cancer: Circulating Immune-Related Biomarkers
Głuszko, A., Szczepański, M. J., Ludwig, N., Mirza, S. M., & Olejarz, W. (2019) · BioMed Research International · doi:10.1155/2019/1628029 · Cited by 45
Li, Y., Zhang, H., Fan, L., Mou, J., Yin, Y., Peng, C., Chen, Y., Lu, H., Zhao, L., Tao, Z., et al. (2020) · Oncogene · doi:10.1038/s41388-020-1228-1 · Cited by 44
Extracellular Vesicles: Messengers of p53 in Tumor–Stroma Communication and Cancer Metastasis
Pavlakis, E., Neumann, M. M., & Stiewe, T. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249648 · Cited by 45
Regulators at Every Step—How microRNAs Drive Tumor Cell Invasiveness and Metastasis
Grzywa, T. M., Klicka, K., & Wlodarski, P. K. (2020) · Cancers · doi:10.3390/cancers12123709 · Cited by 46
Jahan, S., Mukherjee, S., Ali, S., Bhardwaj, U., Choudhary, R. K., Balakrishnan, S., Naseem, A., Mir, S. A., Banawas, S., Alaidarous, M., et al. (2022) · Cells · doi:10.3390/cells11030490 · Cited by 47
Zhao, D., Wu, K., Sharma, S., Xing, F., Wu, S.-Y., Tyagi, A., Deshpande, R. P., Singh, R. N., Wabitsch, M., Mo, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35305-2 · Cited by 45
Extracellular vesicles and melanoma: New perspectives on tumor microenvironment and metastasis
Benito‐Martín, A., Jasiulionis, M. G., & Garcı́a-Silva, S. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1061982 · Cited by 48
Inflammatory microenvironment and human papillomavirus-induced carcinogenesis
Mangino, G., Chiantore, M. V., Iuliano, M., Fiorucci, G., & Romeo, G. (2016) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2016.03.007 · Cited by 44
Cesi, G., Walbrecq, G., Margue, C., & Kreis, S. (2016) · Cell Communication and Signaling · doi:10.1186/s12964-016-0136-z · Cited by 47
The Diverse Oncogenic and Tumor Suppressor Roles of microRNA-105 in Cancer
Li, J., Zhang, Z., Chen, F., Hu, T., Peng, W., Gu, Q., & Sun, Y. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.00518 · Cited by 44
Roles of exosomes in metastatic colorectal cancer
Lafitte, M., Lecointre, C., & Roche, S. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00218.2019 · Cited by 45
Genes that Mediate Metastasis across the Blood–Brain Barrier
Fares, J., Kanojia, D., Rashidi, A., Ulasov, I. V., & Lesniak, M. S. (2020) · Trends in cancer · doi:10.1016/j.trecan.2020.04.007 · Cited by 45
Zheng, X. F. S., Lu, S., He, Z., Huang, H., Yao, Z., Miao, Y., Cai, C., & Zou, F. (2020) · Oncogene · doi:10.1038/s41388-020-01514-6 · Cited by 44
Recent Advances on Extracellular Vesicles in Central Nervous System Diseases
Jin, T., Gu, J., Li, Z., Xu, Z., & Gui, Y. (2021) · Clinical Interventions in Aging · doi:10.2147/cia.s288415 · Cited by 44
Self-citationVillanueva, J. P., Agudo, J. T., & Borau, J. M. (2013) · Biology · doi:10.3390/biology · Cited by 44
Ma, Y., Wu, T., Lv, Z., Lu, G., Cong, X., Xie, R., Yang, H., Chang, Z., Sun, R., Chai, L., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.14435 · Cited by 43
Pallarès-Rusiñol, A., Bernuz, M., Moura, S. L., Fernández-Senac, C., Rossi, R., Martí, M., & Pividori, M. I. (2022) · Advances in clinical chemistry · doi:10.1016/bs.acc.2022.09.002 · Cited by 49
Liu, K., Dou, R., Yang, C., Di, Z., Shi, D., Zhang, C., Song, J., Fang, Y., Huang, S., Xiang, Z., et al. (2023) · Carcinogenesis · doi:10.1093/carcin/bgad013 · Cited by 43
Wang, S., Wu, W., Lin, X., Zhang, K. M., Wu, Q., Luo, M., & Zhou, J. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-01171-8 · Cited by 47
“The roles of miRNA-105 and miRNA-200 in extracellular vesicles produced by breast cancer in the pre-metastatic microenvironment still require further investigation [21–23].”
BackgroundDeterminants of Organotropic Metastasis
Smith, H. A., & Kang, Y. (2016) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-041916-064715 · Cited by 47
Che, S. P. Y., Park, J. Y., & Stokol, T. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00261 · Cited by 43
Ferguson, S. W., Kim, S., Lee, C., Deci, M. B., & Nguyen, J. (2018) · The AAPS Journal · doi:10.1208/s12248-018-0227-4 · Cited by 47
Okamoto, M., Fukushima, Y., Kouwaki, T., Daito, T., Kohara, M., Kida, H., & Oshiumi, H. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.003862 · Cited by 45
The Extracellular Matrix and Vesicles Modulate the Breast Tumor Microenvironment
Yang, J., Bahçecioğlu, G., & Zorlutuna, P. (2020) · Bioengineering · doi:10.3390/bioengineering7040124 · Cited by 42
Dietary microRNAs and cancer: A new therapeutic approach?
Dávalos, A., Pinilla, L., Hazas, M. L. D. L., Pinto-Hernández, P., Barbé, F., Iglesias‐Gutiérrez, E., & de Gonzalo‐Calvo, D. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.10.006 · Cited by 42
Uncovering temperature‐dependent extracellular vesicle secretion in breast cancer
Otsuka, K., Yamamoto, Y., & Ochiya, T. (2020) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12049 · Cited by 41
Wang, C., Wang, J., Shen, X., Li, M., Yue, Y., Cheng, X., Lü, W., Wang, X., & Xie, X. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-01899-6 · Cited by 43
Wang, M., Zhao, M., Guo, Q., Lou, J., & Wang, L. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112834 · Cited by 43
Engineered exosomes for cancer theranostics: Next-generation tumor targeting
Chavda, V. P., Sugandhi, V. V., Pardeshi, C. V., Patil, R., Joshi, M., Patel, B. M., Khadela, A. D., Bezbaruah, R., Bhattacharjee, B., Balar, P. C., et al. (2023) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2023.104579 · Cited by 44
Extracellular Vesicles and Vascular Injury: New Insights for Radiation Exposure
Flamant, S., & Tamarat, R. (2016) · Radiation Research · doi:10.1667/rr14482.1 · Cited by 44
“miR-132 HUVECs p120RASGAP/RASA1 Pro-angiogenic in vitro (125) miR-105 HMVECs TJP1/ZO-1 Increased cell migration and vascular permeability in vitro and in vivo (126)”
Otsuka, K., Yamamoto, Y., Matsuoka, R., & Ochiya, T. (2017) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201700080 · Cited by 43
Extracellular Vesicles As miRNA Nano-Shuttles: Dual Role in Tumor Progression
Pucci, M., Reclusa, P., Duréndez-Saéz, E., Lewintre, E. J., Malarani, M., Khan, S., Fontana, S., Naing, A., Passiglia, F., Raez, L. E., et al. (2018) · Targeted Oncology · doi:10.1007/s11523-018-0551-8 · Cited by 43
Celastrol induces ubiquitin-dependent degradation of mTOR in breast cancer cells
Li, X., Guangbei, Z., Yao, X., Wang, N., Hu, R., Kong, Q., Zhou, D., Long, L., Cai, J., & Zhou, W. (2018) · OncoTargets and Therapy · doi:10.2147/ott.s187315 · Cited by 43
Albacete-Albacete, L., Sánchez‐Álvarez, M., & del Pozo, M. Á. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.671485 · Cited by 43
Tumor extracellular vesicles drive metastasis (it's a long way from home)
Ghoroghi, S., Mary, B., Asokan, N., Goetz, J. G., & Hyenne, V. (2021) · FASEB BioAdvances · doi:10.1096/fba.2021-00079 · Cited by 45
Cancer-derived exosomes as novel biomarkers in metastatic gastrointestinal cancer
Zhong, D., Wang, Z., Ye, Z., Wang, Y., & Cai, X. (2024) · Molecular Cancer · doi:10.1186/s12943-024-01948-6 · Cited by 41
“Zhou et al. reported that miR-105-containing exosomes efficiently destroy the tight junctions and integrity of endothelial monolayers to reach ideal organs to increase vascular permeability, thereby facilitating metastasis [40].”
BackgroundBrain metastasis: New opportunities to tackle therapeutic resistance
Seoane, J., & Mattos‐Arruda, L. D. (2014) · Molecular Oncology · doi:10.1016/j.molonc.2014.05.009 · Cited by 41
Jin, H., Wu, Y., & Tan, X. (2017) · Clinical & Translational Oncology · doi:10.1007/s12094-017-1625-2 · Cited by 42
Taverna, S., Giusti, I., D’Ascenzo, S., Pizzorno, L., & Dolo, V. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103573 · Cited by 40
SRSF1 regulates exosome microRNA enrichment in human cancer cells
Xu, Y., Xu, X., Gin, A. L., Nshimiyimana, J. D., Mooers, B. H. M., Caputi, M., Hannafon, B. N., & Ding, W. (2020) · Cell Communication and Signaling · doi:10.1186/s12964-020-00615-9 · Cited by 43
Metadata
- Authors
- Zhou, W., Fong, M. Y., Min, Y., Somlo, G., Liu, L., Palomares, M. R., Yu, Y., Chow, A., O’Connor, S. T. F., Chin, A. R., Yen, Y., Wang, Y., Marcusson, E. G., Chu, P., Wu, J., Wu, X., Li, A. X., Li, Z., Gao, H., Ren, X., Boldin, M. P., Lin, P. C., & Wang, S. E.
- Affiliations
- City Of Hope National Medical Center (US)
- National Cancer Institute (US)
- Regulus Therapeutics (United States) (US)
- Tianjin Medical University Cancer Institute and Hospital (CN)
- Corresponding author
- Wang, Shizhen Emily
- ORCID
- Venue
- Cancer Cell
- Publisher
- Elsevier BV
- Published
- 2014-04
- Volume
- 25
- Issue
- 4
- Pages
- 501-515
- ISSN
- 1535-6108 (ISSN-L)
- PMC
- PMC4016197
- OpenAlex
- W2143839116
- Cited by
- 1,476
- References
- 62
- Citations by year
- 2026: 61 · 2025: 91 · 2024: 113 · 2023: 145 · 2022: 164 · 2021: 175 · 2020: 148 · 2019: 152 · 2018: 118 · 2017: 111 · 2016: 97 · 2015: 72 · 2014: 28
- FWCI
- 32.89
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cancer Cell (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- American Association for Cancer Research
- Breast Cancer Research Foundation (12-60-26-WANG)
- Celgene
- National Institutes of Health
- National Key Research and Development Program of China (2012CB9333004)
- National Cancer Institute (P30CA-33572, R01CA166020, R01CA163586, P30CA033572)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
- Keywords
- miR-105, metastasis, breast cancer, ZO-1, tight junctions, endothelial barrier integrity, exosomes, vascular permeability, metastatic progression
- MeSH terms
- Breast Neoplasms, Cell Movement, Endothelium, Vascular, Female, Humans, Neoplasm Metastasis, Biomarkers, Tumor, MicroRNAs, Cell Line, Tumor, Cell Growth Processes
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