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MicroRNAs as the fine-tuners of Src oncogenic signalling
被引:15
|作者:
Oneyama, Chitose
[1
,2
]
Okada, Masato
[2
]
机构:
[1] Aichi Canc Ctr Res Inst, Div Microbiol & Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Dept Oncogene Res, Suita, Osaka 5650871, Japan
来源:
关键词:
cancer signalling;
microRNA;
mTOR;
proto-oncogene;
Src;
INTEGRIN-LINKED KINASE;
CELL LUNG-CANCER;
TUMOR-SUPPRESSOR;
PROSTATE-CANCER;
TYROSINE PHOSPHORYLATION;
GEFITINIB RESISTANCE;
MIRNA EXPRESSION;
ADAPTER PROTEIN;
FAMILY KINASES;
C-SRC;
D O I:
10.1093/jb/mvv036
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The cellular Src (c-Src) tyrosine kinase is upregulated and believed to play a pivotal role in various human cancers. However, the molecular mechanism underlying c-Src-mediated tumour progression remains elusive. Recent studies have revealed that several microRNAs (miRNAs) function as tumour suppressors by regulating the malignant expression of signalling molecules. Aberrant expression of miRNAs is frequently observed in human cancers and should be exploited to seek related molecular targets. In this review, we focus on miRNAs found to be involved in Src signalling in various cancers. We summarize recent findings on Src-related miRNAs, their target genes, mechanisms behind their interplay and their implications for cancer therapeutics.
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页码:431 / 438
页数:8
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