4.6 Article

HSPB1 rs2070804 polymorphism is associated with the depth of primary tumor

期刊

JOURNAL OF CELLULAR BIOCHEMISTRY
卷 121, 期 1, 页码 63-69

出版社

WILEY
DOI: 10.1002/jcb.28266

关键词

colon cancer; heat shock protein beta-1 (HSPB1); metastasis; polymorphism; tumor

资金

  1. Ministry of Science and Technology, Taiwan [MOST107-2321-B-037-003, MOST107-2314-B-037-116, MOST107-2314-B-037-022-MY2, MOST107-2314-B-037-023-MY2]
  2. Ministry of Health and Welfare [MOHW106-TDU-B-212-113006, MOHW107-TDU-B-212-123006, MOHW107-TDU-B-212-114026B]
  3. Health and welfare surcharge of tobacco products
  4. Grant of Biosignature in Colorectal Cancers, Academia Sinica, Taiwan, R.O.C.

向作者/读者索取更多资源

Background Colorectal cancer (CRC) is the third most common cancer in the world. Genome-wide association studies are a powerful method to analyze the status of single-nucleotide polymorphisms (SNPs) in specific genes. Heat shock proteins (HSPs) were found to be involved in the cancer progression and chemoresistance. However, there is still no further study about polymorphisms of HSP beta-1 (HSPB1) in colorectal cancer. We proposed the SNP of HSPB1 may be correlated with the progression and metastasis in colon cancer. Methods We recruited 379 colorectal cancer patients and categorized as four stages following the UICC TNM system. Then, we selected tagging SNPs of HSPB1 by 10% minimum allelic frequency in Han Chinese population from the HapMap database and analyze with the Chi-square test. Results We demonstrated the association of HSPB1 genetic polymorphisms rs2070804 with tumor depth with colorectal cancer. But, there is a lack of association between HSPB1 genetic polymorphisms and colorectal cancer invasion, recurrence or metastasis. Conclusions The polymorphisms of HSPB1 seemed to change the tumor behavior of colorectal cancer. HSPB1 rs2070804 polymorphism is associated with the depth of the primary tumor. But, there is no further correlation with other to the clinical parameters such as cancer invasiveness, local recurrence, or distant metastasis.

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