Deregulation of miR-۲۱ and miR-۱۵۵ and their putative targets after silibinin treatment in T۴۷D breast cancer cells

Publish Year: 1394
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:

JR_IJBMS-18-12_007

تاریخ نمایه سازی: 3 آبان 1400

Abstract:

Objective(s):MicroRNAs (miRNAs) are a class of short RNAs that control the biological processes including cell proliferation, apoptosis and development. Aberrant expression of miRNAs was determined in the different stages of tumor development and metastasis. To study the effect of silibinin on miRNAs expression, we evaluated quantitative expression of miR-۲۱ and miR-۱۵۵ as two oncomiRs and several potential targets in silibinin-treated T۴۷D cells. Materials and Methods:The rate of proliferation and apoptosis was measured in silibinin-treated and untreated cells. The expression levels of miR-۲۱ and miR-۱۵۵ were evaluated in T۴۷D cells treated with silibinin (۱۰۰ µg/ml). Also, their putative targets were predicted in apoptotic pathways using multiple algorithms; as a confirmation, the transcription level of APAF-۱, CASP-۹ and BID was evaluated. Results:In silibinin-treated cells, death was occurred in a dose and time-dependent manner. miR-۲۱ and miR-۱۵۵ was downregulated in cells treated with silibinin (۱۰۰ µg/ml). It is noticeable that the expression of their potential targets including CASP-۹ and APAF-۱ was increased in silibinin-treated cells after ۴۸ hr. Conclusion:Our findings showed a correlation between the expression of miR-۲۱ and miR-۱۵۵ and apoptosis in silibinin treated T۴۷D cells. It seems that miRNAs such as miR-۲۱ and miR-۱۵۵ were regulated by silibinin. Also, increase in the transcript level of APAF-۱ and CASP-۹ after downregulation of miR-۲۱ and miR-۱۵۵ might indicate that these genes were targeted by aforementioned miRNAs in T۴۷D cells.

Authors

Masoud Maleki Zadeh

Department of Cell and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran

Najmeh Ranji

Department of Genetics, College of Science, Rasht Branch, Islamic Azad University, Rasht, Iran

Nasrin Motamed

Department of Cell and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran

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  • Noh EM, Yi MS, Youn HJ, Lee BK, Lee YR, ...
  • Lee SO, Jeong YJ, Im HG, Kim CH, Chang YC, ...
  • Nasiri M, Zarghami N, Koshki KN, Mollazadeh M, Moghaddam MP, ...
  • Hsieh YS, Chu SC, Yang SF, Chen PN, Liu YC, ...
  • Ranji N, Sadeghizadeh M, Shokrgozar MA, Bakhshandeh B, Karimipour M, ...
  • Calin GA, Croce CM. MicroRNA signatures in human cancers. Nat ...
  • Tili E, Michaille JJ, Calin GA. Expression and function of ...
  • Selbach M, Schwanhausser B, Thierfelder N, Fang Z, Khanin R, ...
  • Ruan K, Fang X, Ouyang G. MicroRNAs: novel regulators in ...
  • Lechman ER, Gentner B, van Galen P, Giustacchini A, Saini ...
  • Shimizu S, Takehara T, Hikita H, Kodama T, Miyagi T, ...
  • Yang M, Li Y, Padgett RW. MicroRNAs: Small regulators with ...
  • Wang Z, Li Y, Kong D, Ahmad A, Banerjee S, ...
  • Lal A, Navarro F, Maher CA, Maliszewski LE, Yan N, ...
  • Cho WC. OncomiRs: the discovery and progress of microRNAs in ...
  • Johnson CD, Esquela-Kerscher A, Stefani G, Byrom M, Kelnar K, ...
  • Sarkar FH, Li Y, Wang Z, Kong D, Ali S. ...
  • Yang H, Kong W, He L, Zhao JJ, O'Donnell JD, ...
  • Chen YH, Chen CL, Liang CM, Liang JB, Tai MC, ...
  • Kil WH, Kim SM, Lee JE, Park KS, Nam SJ. ...
  • Ting H, Deep G, Agarwal R. Molecular mechanisms of silibinin-mediated ...
  • Wang ZX, Lu BB, Wang H, Cheng ZX, Yin YM. ...
  • Babashah S, Sadeghizadeh M, Hajifathali A, Tavirani MR, Zomorod MS, ...
  • Yan LX, Huang XF, Shao Q, Huang MY, Deng L, ...
  • Iorio MV, Ferracin M, Liu CG, Veronese A, Spizzo R, ...
  • Jiang S, Zhang LF, Zhang HW, Hu S, Lu MH, ...
  • Gan R, Yang Y, Yang X, Zhao L, Lu J, ...
  • Chen WX, Hu Q, Qiu MT, Zhong SL, Xu JJ, ...
  • Andorfer CA, Necela BM, Thompson EA, Perez EA. MicroRNA signatures: ...
  • Negrini M, Nicoloso MS, Calin GA. MicroRNAs and cancernew paradigms ...
  • Selcuklu SD, Donoghue MT, Spillane C. miR-۲۱ as a key ...
  • Mattiske S, Suetani RJ, Neilsen PM, Callen DF. The oncogenic ...
  • Zhang CM, Zhao J, Deng HY. MiR-۱۵۵ promotes proliferation of ...
  • Ekimler S, Sahin K. Computational methods for microRNA target prediction. ...
  • Frankel LB, Christoffersen NR, Jacobsen A, Lindow M, Krogh A, ...
  • Higgs G, Slack F. The multiple roles of microRNA-۱۵۵ in ...
  • Fu WN, Bertoni F, Kelsey SM, McElwaine SM, Cotter FE, ...
  • Kamarajan P, Sun NK, Sun CL, Chao CC. Apaf-۱ overexpression ...
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