2020
DOI: 10.1016/j.gene.2019.144268
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What is the impact of BIRC5 gene polymorphisms on urinary cancer susceptibility? Evidence from 9348 subjects

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Cited by 5 publications
(4 citation statements)
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“…In a study on the anticancer properties of FZD7 after pharmacological inhibition of HCC, it was suggested that the mechanism may be associated with PRKCD mutations (32). BIRC5 has been described as a negative regulator of apoptosis, and its expression was reported to be higher in most tumors including HCC (33)(34)(35)(36), which is consistent with our findings indicating that the expression of BIRC5 is higher in the high-risk group of HCC prognosis. Moreover, the potential influence of BIRC5, HMOX1, and VEGFA in the prognosis of HCC had been reported in studies by Wang et al(37), Shen et al (38), and…”
Section: Discussionsupporting
confidence: 91%
“…In a study on the anticancer properties of FZD7 after pharmacological inhibition of HCC, it was suggested that the mechanism may be associated with PRKCD mutations (32). BIRC5 has been described as a negative regulator of apoptosis, and its expression was reported to be higher in most tumors including HCC (33)(34)(35)(36), which is consistent with our findings indicating that the expression of BIRC5 is higher in the high-risk group of HCC prognosis. Moreover, the potential influence of BIRC5, HMOX1, and VEGFA in the prognosis of HCC had been reported in studies by Wang et al(37), Shen et al (38), and…”
Section: Discussionsupporting
confidence: 91%
“…For rs9904341 (c.-31G>C), the major G allele and GG genotype were associated with positive lymph nodes and higher TNM status in this study. This polymorphism is the most studied BIRC5 polymorphism [28] and the subject of several meta-analyses [29][30][31]. It is located in the 5 ′ UTR region of the BIRC5 gene and modifies the binding motif of the CDE/CHR repressor [27].…”
Section: Discussionmentioning
confidence: 99%
“…It is located in the 5 ′ UTR region of the BIRC5 gene and modifies the binding motif of the CDE/CHR repressor [27]. It has been associated with susceptibility (oral [15,32], esophageal [16,33], colorectal [17,34,35], lung [14], and urinary tract cancers [22,31,[36][37][38][39][40]), survival (colorectal [17] and lung cancers [41]), and age of onset (ovarian [19] and prostate cancers [42]). As in this study, an association was also found with stage and lymph node status (oral [43,44], esophageal [33], pancreatic [45], urinary [36,38,39], lung [46], and colorectal cancers [34]).…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, studies provide support that paracrine IGF1/IGF1R signaling promotes colorectal cancer progression [ 26 , 27 ].Regulation of TFGBR3 contributes to the development of pancreatic ductal adenocarcinoma and metastasis of clear-cell renal cell carcinoma [28] .The expression of MASP-1 is down-regulated in the tumor samples compared to normal samples from GEO datasets. It's reported that MASP-1 serum levels are associated with worse prognostic in cervical cancer progression [29] .A meta-analysis reveals that several polymorphisms of BIRC5, a member of apoptosis inhibition gene family, might cause the different risk of urinary cancer [30] .…”
Section: Discussionmentioning
confidence: 99%