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MicroRNAs in apoptosis, autophagy and necroptosis
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// Zhenyi Su 1, 2, * , Zuozhang Yang 3, 4, * , Yongqing Xu 4, * , Yongbin Chen 5, * , Qiang Yu 6, * 1 Department of Biochemistry and Molecular Biology, Medical School, Southeast University, Nanjing, Jiangsu 210009, China 2 Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA 3 Bone and Soft Tissue Tumors Research Center of Yunnan Province, Department of Orthopaedics, the Third Affiliated Hospital of Kunming Medical University (Tumor Hospital of Yunnan Province), Kunming, Yunnan 650118, China 4 Department of Orthopaedics, Kunming General Hospital of Chengdu Military Command, Kunming, Yunnan 650118, China 5 Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China 6 Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China * These authors have contributed equally to this work Correspondence to: Zuozhang Yang, e-mail: yangzuozhang@163.com Keywords: microRNA, apoptosis, autophagy, necroptosis, cancer progression Received: February 02, 2015 Accepted: March 10, 2015 Published: April 02, 2015 ABSTRACT MicroRNAs (miRNAs) are endogenous 22 nt non-coding RNAs that target mRNAs for cleavage or translational repression. Numerous miRNAs regulate programmed cell death including apoptosis, autophagy and necroptosis. We summarize how miRNAs regulate apoptotic, autophagic and necroptotic pathways and cancer progression. We also discuss how miRNAs link different types of cell death.
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Curcumin promotes apoptosis in human lung adenocarcinoma cells through miR-186* signaling pathway
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Hamada, S., Masamune, A., Miura, S., Satoh, K., & Shimosegawa, T. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.11.003 · Cited by 136
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MicroRNA-155 prevents necrotic cell death in human cardiomyocyte progenitor cells via targeting RIP1
Liu, J., van Mil, A., Vrijsen, K. R., Zhao, J., Gao, L., Metz, C. H. G., Goumans, M., Doevendans, P. A., & Sluijter, J. P. G. (2010) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2010.01104.x · Cited by 123
miR-148b Functions as a Tumor Suppressor in Pancreatic Cancer by Targeting AMPKα1
Zhao, G., Zhang, J., Liu, Y., Qin, Q., Wang, B., Tian, K., Liu, L., Li, X., Niu, Y., Deng, S., et al. (2012) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-12-0534-t · Cited by 121
microRNA-24a is required to repress apoptosis in the developing neural retina
McGann, J. C., & Harland, R. M. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.05.197 · Cited by 119
A CHOP-regulated microRNA controls rhodopsin expression
Behrman, S. L., Acosta‐Alvear, D., & Walter, P. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201010055 · Cited by 113
Huang, Y., Guerrero-Preston, R. E., & Ratovitski, E. A. (2012) · Cell Cycle · doi:10.4161/cc.11.6.19670 · Cited by 111
Core signaling pathways of survival/death in autophagy-related cancer networks
Wang, S., Yu, Q., Zhang, R., & Liu, B. (2011) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2011.05.010 · Cited by 111
Self-citationmiR-874 regulates myocardial necrosis by targeting caspase-8
Wang, K., Liu, F., Zhou, L.-Y., Ding, S.-L., Long, B., Liu, C.-Y., Sun, T., Fan, Y.-Y., Sun, L., & Li, P.-F. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.233 · Cited by 110
Oneyama, C., Ikeda, J., Okuzaki, D., Suzuki, K., Kanou, T., Shintani, Y., Morii, E., Okumura, M., Aozasa, K., & Okada, M. (2011) · Oncogene · doi:10.1038/onc.2011.63 · Cited by 106
Cai, N., Wang, Y., & Zheng, P. (2012) · RNA · doi:10.1261/rna.035295.112 · Cited by 103
SnapShot: Extrinsic Apoptosis Pathways
Verbrugge, I., Johnstone, R. W., & Smyth, M. J. (2010) · Cell · doi:10.1016/j.cell.2010.12.004 · Cited by 101
Shi, Y., Chen, C., Zhang, X., Liu, Q., Xu, J., Zhang, H., Yao, X., Jiang, T., He, Z., Ren, Y., et al. (2014) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-2284 · Cited by 101
Ye, D., Wang, G., Liu, Y., Huang, W., Wu, M., Zhu, S., Jia, W., Deng, A., Liu, H., & Kang, J. (2012) · Stem Cells · doi:10.1002/stem.1149 · Cited by 99
Hudson, R. S., Yi, M., Esposito, D., Glynn, S. A., Starks, A. M., Yang, Y., Schetter, A. J., Watkins, S. K., Hurwitz, A. A., Dorsey, T. H., et al. (2013) · Oncogene · doi:10.1038/onc.2012.424 · Cited by 98
MicroRNA-24 regulates XIAP to reduce the apoptosis threshold in cancer cells
Xie, Y., Tobin, L. A., Camps, J., Wangsa, D., Yang, J., Rao, M., Witasp, E., Awad, K. S., Yoo, N., Ried, T., et al. (2012) · Oncogene · doi:10.1038/onc.2012.258 · Cited by 98
MicroRNA-608 and MicroRNA-34a Regulate Chordoma Malignancy by Targeting EGFR, Bcl-xL and MET
Zhang, Y., Schiff, D., Park, D. M., & Abounader, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091546 · Cited by 98
Ichimura, A., Ruike, Y., Terasawa, K., Shimizu, K., & Tsujimoto, G. (2010) · Molecular Pharmacology · doi:10.1124/mol.109.063321 · Cited by 94
YANG, G., Wu, D., Zhu, J., Jiang, O., Shi, Q., Tian, J., & Weng, Y. (2013) · Oncology Reports · doi:10.3892/or.2013.2532 · Cited by 93
MiR‐503 targets PI3K p85 and IKK‐β and suppresses progression of non‐small cell lung cancer
Yang, Y., Liu, L., Zhang, Y., Guan, H., Wu, J., Zhu, X., Yuan, J. X., & Li, M. (2014) · International Journal of Cancer · doi:10.1002/ijc.28799 · Cited by 92
MiR‐483–5p suppresses the proliferation of glioma cells via directly targeting ERK1
Wang, L., Shi, M., Hou, S., Ding, B., Liu, L., Ji, X., Zhang, J., & Deng, Y. (2012) · FEBS Letters · doi:10.1016/j.febslet.2012.03.035 · Cited by 87
Srivastava, N., Manvati, S., Srivastava, A., Pal, R., Ponnusamy, K., Chattopadhyay, S., Gochhait, S., Dua, R., & Bamezai, R. N. K. (2011) · Breast Cancer Research · doi:10.1186/bcr2861 · Cited by 86
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MicroRNA-1826 targets VEGFC, beta-catenin (CTNNB1) and MEK1 (MAP2K1) in human bladder cancer
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miR-210 suppresses BNIP3 to protect against the apoptosis of neural progenitor cells
Wang, F., Xiong, L., Huang, X. H., Zhao, T., Wu, L., Liu, Z., Ding, X., Liu, S., Wu, Y., Zhao, Y., et al. (2013) · Stem Cell Research · doi:10.1016/j.scr.2013.04.005 · Cited by 80
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Autophagy: Regulation by Energy Sensing
Meijer, A. J., & Codogno, P. (2011) · Current Biology · doi:10.1016/j.cub.2011.02.007 · Cited by 77
microRNA30Apromotes autophagy in response to cancer therapy
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Guo, Q., Zhang, J., Li, J., Zou, L., Zhang, J., Xie, Z., Fu, X., Jiang, S., Chen, G., Jia, Q., et al. (2013) · Blood · doi:10.1182/blood-2012-08-452425 · Cited by 66
miR-155 Suppresses Bacterial Clearance in Pseudomonas aeruginosa–Induced Keratitis by Targeting Rheb
Yang, K., Wu, M., Li, M., Li, D., Peng, A., Nie, X., Sun, M., Wang, J., Wu, Y., Deng, Q., et al. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu002 · Cited by 59
MicroRNA 203 Modulates Glioma Cell Migration via Robo1/ERK/MMP-9 Signaling
Dontula, R., Dinasarapu, A. R., Chetty, C., Pannuru, P., Herbert, E., Ozer, H., & Lakka, S. S. (2013) · Genes & Cancer · doi:10.1177/1947601913500141 · Cited by 57
Yamada, N. O., Noguchi, S., Kumazaki, M., Shinohara, H., Miki, K., Naoe, T., & Akao, Y. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.11.022 · Cited by 53
Synthetic pre-microRNAs reveal dual-strand activity of miR-34a on TNF-α
Guennewig, B., Roos, M. M., Dogar, A. M., Gebert, L. F. R., Zagalak, J. A., Vongrad, V., Metzner, K. J., & Hall, J. (2013) · RNA · doi:10.1261/rna.038968.113 · Cited by 53
The microRNA and p53 families join forces against cancer
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MicroRNA-17 inhibits tumor growth by stimulating T-cell mediated host immune response
Li, H., Gupta, S., Du, W. W., & Yang, B. B. (2014) · Oncoscience · doi:10.18632/oncoscience.69 · Cited by 35
Sánchez-Díaz, P. C., Hsiao, T.-H., Zou, Y., Sugalski, A., Heim-Hall, J. M., Chen, Y., Langevin, A., & Hung, J. Y. (2014) · Oncoscience · doi:10.18632/oncoscience.85 · Cited by 28
Self-citationJu, J.-A., Huang, C.-T., Lan, S., Wang, T.-H., Lin, P., Lee, J.-C., Tian, Y.-F., & Liu, H. (2013) · Biomarkers and Genomic Medicine · doi:10.1016/j.bgm.2013.07.006 · Cited by 22
Martin, E. C., Krebs, A. E., Burks, H. E., Elliott, S. G., Baddoo, M., Collins‐Burow, B. M., Flemington, E. K., & Burow, M. E. (2014) · Genes & Cancer · doi:10.18632/genesandcancer.33 · Cited by 20
microRNAs: short non-coding bullets of gain of function mutant p53 proteins
Donzelli, S., Strano, S., & Blandino, G. (2014) · Oncoscience · doi:10.18632/oncoscience.52 · Cited by 19
Apoptosis, Cell Signaling, and Human Diseases
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Programmed Necrosis/Necroptosis: An Inflammatory Form of Cell Death
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Regulation of Metastasis by miRNAs
Alahari, S. K. (2012) · Springer eBooks · doi:10.1007/978-94-007-4655-8_6 · Cited by 1
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Programmed cell death in spinal cord injury pathogenesis and therapy
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Scioli, M. G., Storti, G., D’Amico, F., Rodríguez Guzmán, R., Centofanti, F., Doldo, E., Céspedes Miranda, E. M., & Orlandi, A. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9061995 · Cited by 281
MiR-137: an important player in neural development and neoplastic transformation
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Metadata
- Authors
- Su, Z., Yang, Z., Xu, Y., Chen, Y., & Yu, Q.
- Venue
- Oncotarget
- Publisher
- Impact Journals, LLC
- Published
- 2015-04-02
- Volume
- 6
- Issue
- 11
- Pages
- 8474-8490
- ISSN
- 1949-2553 (ISSN-L)
- OpenAlex
- W1945652054
- Cited by
- 342
- References
- 141
- FWCI
- 13.44
- Type
- journal article
- Language
- en
- Open access
- diamond
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.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.