miR-335-5p suppresses gastric cancer progression by targeting MAPK10.
miR-335-5p suppresses gastric cancer progression by targeting MAPK10.
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DOI:
10.1186/s12935-020-01684-z
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发表时间:
2021-01-22
影响因子:
5.8
通讯作者:
Zhang J
中科院分区:
文献类型:
--
作者:
Gao Y;Wang Y;Wang X;Zhao C;Wang F;Du J;Zhang H;Shi H;Feng Y;Li D;Yan J;Yao Y;Hu W;Ding R;Zhang M;Wang L;Huang C;Zhang J
Recent studies have established the roles of microRNAs (miRNAs) in cancer progression. The aberrant expression of miR-335-5p has been reported in many cancers, including gastric cancer (GC). In this study, the precise roles of miR-335-5p in GC as well as the molecular mechanisms underlying its effects, including the role of its target MAPK10, were evaluated. Quantitative real-time PCR was used to evaluate miR-335-5p levels in GC cell lines and tissues. MTT and colony formation assays were used to detect cell proliferation, and Transwell and wound-healing assays were used to evaluate the invasion and migration of GC cells. The correlation between levels of miR-335-5p and the cell cycle-related target gene mitogen-activated protein kinase 10 (MAPK10) in GC was analyzed. In addition, the candidate target was evaluated by a luciferase reporter assay, qRT-PCR, and western blotting. The levels of miR-335-5p were downregulated in GC tissues and cell lines. Furthermore, miR-335-5p inhibited the proliferation and migration of GC cells and induced apoptosis. Additionally, miR-335-5p arrested the cell cycle at the G1/S phase in GC cells in vitro. Levels of miR-335-5p and the cell cycle-related target gene MAPK10 in GC were correlated, and MAPK10 was directly targeted by miR-335-5p. These data suggest that miR-335-5p is a tumor suppressor and acts via MAPK10 to inhibit GC progression.
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影响因子:
6.4
作者:
Slattery, Martha L.;Herrick, Jennifer S.;Mullany, Lila E.;Valeri, Nicola;Stevens, John;Caan, Bette J.;Samowitz, Wade;Wolff, Roger K.
通讯作者:
Wolff, Roger K.
影响因子:
4.6
作者:
Kahraman M;Röske A;Laufer T;Fehlmann T;Backes C;Kern F;Kohlhaas J;Schrörs H;Saiz A;Zabler C;Ludwig N;Fasching PA;Strick R;Rübner M;Beckmann MW;Meese E;Keller A;Schrauder MG
通讯作者:
Schrauder MG
DOI:
10.26355/eurrev_201907_18429
发表时间:
2019-07-01
影响因子:
3.3
作者:
Shang, J-C;Yu, G-Z;Xia, L.
通讯作者:
Xia, L.
影响因子:
14.9
作者:
Liu Q;Fu H;Sun F;Zhang H;Tie Y;Zhu J;Xing R;Sun Z;Zheng X
通讯作者:
Zheng X
影响因子:
11.2
作者:
Citron, Francesca;Segatto, Ilenia;Belletti, Barbara
通讯作者:
Belletti, Barbara