The Role of Formyl Peptide Receptor 1 Gene Polymorphisms in Human Colorectal Cancer
The Role of Formyl Peptide Receptor 1 Gene Polymorphisms in Human Colorectal Cancer
复制标题
甲酰基肽受体1基因多态性在人结直肠癌中的作用
DOI:
10.7150/jca.36355
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发表时间:
2020-03
影响因子:
3.9
通讯作者:
Ning Su
中科院分区:
文献类型:
--
作者:
Shu-Qin Li;Yang Yu;Yan Zhang;Yan-Ping Sun;Xin-xing Li;Ning Su
Formyl peptide receptor 1 (FPR1) belongs to G protein-coupled receptors expressed mainly in phagocytic leukocytes. The gene encoding FPR1 is highly polymorphic and related to inflammation. In this study, we investigated the single nucleotide polymorphisms (SNPs) of Fpr1 in human colorectal cancer (CRC), and analyzed the association of Fpr1 SNPs with clinicopathological parameters and some specific diagnostic markers of CRC. Although the allele and genotype frequencies of Fpr1 SNPs in CRC tissues were not significantly different from that in whole blood cells derived from healthy Chinese subjects. Significant associations were observed between genotypes of c.289C>A and distant metastasis (P=0.001), and between genotypes of c.306T>C and tumor size (P=0.016). Genotypes of c.546C>A was closer to tumor size and lymphatic invasion (P=0.012 and P=0.043, respectively). Meanwhile, genotypes of c.1037C>A was related with tumor location and differentiation (P=0.000 and P=0.005, respectively). Besides, genotypes of c.576T>C>G was related with pathological type (P=0.000). Furthermore, several Fpr1 SNP positions including c.289 (C>A) and c.576 (G>C>T) were related to the expression of P53 (P=0.004 and P=0.008, respectively), and similar results were observed between other Fpr1 SNP positions and CEA, HER2 and Ki-67 (P<0.05). Our data demonstrate that Fpr1 SNPs may play the important role in the progression and metastasis of CRC.
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DOI:
10.1016/b978-1-4160-3251-9.50008-x
发表时间:
2019-10
期刊:
The Lancet
影响因子:
--
作者:
E. Dekker;P. Tanis;J. Vleugels;P. Kasi;M. Wallace
通讯作者:
E. Dekker;P. Tanis;J. Vleugels;P. Kasi;M. Wallace
影响因子:
3.5
作者:
Zhai Cai;Shuai Han;Zhou Li;Lin-yun He;Jiajing Zhou;Wenhua Huang;Yichun Xu
通讯作者:
Zhai Cai;Shuai Han;Zhou Li;Lin-yun He;Jiajing Zhou;Wenhua Huang;Yichun Xu
影响因子:
168.9
作者:
Cunningham, David;Atkin, Wendy;Starling, Naureen
通讯作者:
Starling, Naureen
影响因子:
168.9
作者:
Midgley, R;Kerr, D
通讯作者:
Kerr, D
DOI:
10.1016/j.bbrc.2010.12.136
发表时间:
2011-02
影响因子:
3.1
作者:
T. Otani;S. Ikeda;H. Lwin;T. Arai;M. Muramatsu;M. Sawabe
通讯作者:
T. Otani;S. Ikeda;H. Lwin;T. Arai;M. Muramatsu;M. Sawabe