Association of MHC class-III gene polymorphisms with ER-positive breast cancer in Chinese Han population

Genet Mol Res. 2012 Dec 17;11(4):4299-306. doi: 10.4238/2012.September.17.1.


Polymorphisms of the major histocompatibility complex (MHC) have been linked to many diseases, especially autoimmune disorders. Previous studies have shown that genetic variants in MHC class III are associated with breast cancer. To determine if there is an association between MHC class III and breast cancer risk in the Chinese Han population, we carried out a hospital-based case-control study in Guangdong and Jiangsu Provinces, including 216 histologically confirmed breast cancer patients and 216 healthy controls. Nine SNP markers distributed in the class III-coding region were detected using the Sequenom MassARRAY(®) iPLEX System. Deviation from Hardy-Weinberg equilibrium was observed for seven SNPs. There was no significant association between these seven SNP variants and breast cancer in these Chinese women (unconditional logistic regression analysis). However, chr6_31697494 at BAT2, one of the seven SNPs, was found to be significantly associated with both ER- and PR-positive breast cancer. In addition, both chr6_31911109 at C6orf48 and chr6_31975605 at ZBTB12, another two of the seven SNPs, show relevance with ER-positive breast cancer. In conclusion, this is the first evidence that genetic polymorphisms in the MHC class III region are significantly associated with ER-positive breast cancer in the Han Chinese population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian Continental Ancestry Group
  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism
  • Case-Control Studies
  • DNA-Binding Proteins / genetics*
  • Female
  • Genetic Association Studies
  • Humans
  • Middle Aged
  • Neoplasm Proteins / genetics*
  • Polymorphism, Single Nucleotide*
  • Prognosis
  • Proteins / genetics*
  • Receptors, Estrogen / metabolism*
  • Receptors, Progesterone / metabolism
  • Transcription Factors / genetics*


  • DNA-Binding Proteins
  • Neoplasm Proteins
  • Proteins
  • Receptors, Estrogen
  • Receptors, Progesterone
  • SNHG32 protein, human
  • Transcription Factors
  • ZBTB12 protein, human
  • PRRC2A protein, human