2013
DOI: 10.1016/j.bbrc.2012.12.001
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Genetic variation in a miR-335 binding site in BIRC5 alters susceptibility to lung cancer in Chinese Han populations

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Cited by 33 publications
(18 citation statements)
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“…miR-335 serves as a tumor suppressor miRNA, is transcribed from the genomic region on chromosome 7q32.2 (76) and is downregulated in various human digestive malignancies, such as pancreatic carcinoma, hepatocellular carcinoma, colorectal cancer and gastric cancer (77)(78)(79)(80). A similar result was also observed in GBC patients.…”
Section: Tumor Suppressor Micrornassupporting
confidence: 56%
“…miR-335 serves as a tumor suppressor miRNA, is transcribed from the genomic region on chromosome 7q32.2 (76) and is downregulated in various human digestive malignancies, such as pancreatic carcinoma, hepatocellular carcinoma, colorectal cancer and gastric cancer (77)(78)(79)(80). A similar result was also observed in GBC patients.…”
Section: Tumor Suppressor Micrornassupporting
confidence: 56%
“…SNP rs2239680 in the miR-335 binding site of the oncogene BIRC5 may alter the susceptibility to lung cancer. C allele carriers were found to be predisposed to lung cancer and advanced pathologic stage (Zu et al, 2013). let-7 is one of the most widely studied miRNAs and functions in many biological processes.…”
Section: Discussionmentioning
confidence: 99%
“…gov/cgi-bin/snpinfo/snpfunc.cgi). Combined with other SNPs in the 3'UTR or promoter region, the variant rs2239680 is jointly involved in cancer susceptibility (8,12).…”
Section: Birc5/survivin 3'utr Selected Variants and Putative Mirna Bimentioning
confidence: 99%
“…Zu et al evaluated the association between genetic variants in the 3' untranslated region (3'UTR) of cancer-related genes and risk of lung cancer in Chinese populations, and defined a 3'UTR single nucleotide polymorphism (SNP) in the human BIRC5 oncogene that may increase individual susceptibility to lung cancer, possibly by attenuating the interaction between BIRC5 and miRNA-335 (8). BIRC5/survivin directly binds to the promoter of the miRNA-335 cluster, activating its transcription, and negatively modulating the translation of BIRC5/survivin miRNAs by binding sites in their 3'UTRs (8). In addition, a number of studies have revealed that BIRC5/survivin variants may play crucial roles in carcinogenesis (2).…”
Section: Introductionmentioning
confidence: 99%