Matrix metalloproteinase family gene polymorphisms and lung cancer susceptibility: an updated meta-analysis

Background: Many studies have investigated the association between matrix metalloproteinase polymorphisms and lung cancer susceptibility. However, the results are still controversial. To clarify these associations, we conducted a meta-analysis. Methods: A systematic search of studies was conducted in PubMcd, Embase, and China National Knowledge Infrastructure. Overall and subgroup analysis stratified by ethnicity was conducted. OR with 95% CI was used to assess the strength of the association. Furthermore, false-positive report probability (FPRP) tests were also performed for associations obtained in this meta-analysis. Results: Twenty-four studies, including 10,099 cases and 9,395 controls, were analyzed. Nine polymorphisms were reported. For MMP1 -1607 1G/2G and MMP7 -181 MG, increased lung cancer risk was found in Asians. For MMP2 -1306 Cif and AIMP2 -735 C/T, decreased lung cancer risk was found in both "diverse populations" and Asians. For MIVIP9 -1562, C/T decreased lung cancer risk was found in both "diverse populations" and Caucasians. For MMP13 -77A/G, the A/G genotype decreased lung cancer risk in Asians. However, only associations between MMP1 -1607 1G/2G, MMP2 -1306 Cif, MMP2 -735 C/T, and MMP7 -181 A/G and lung cancer risk were considered noteworthy according to FPRP tests. There was no association between MIVIP3 -1171 5A/6A,1141V1P9 R279Q, and MMP12 -82A/G and lung cancer risk. Conclusions: Our meta-analysis suggested that MMP1-1607 1G/2G and MMP7 -181 MG were risk factors for lung cancer, while MMP2 -1306 C/T, MMP2 -735 C/T, MMP9 -1562 C/T, and MMP13 -77A/G might be protective factors. However, results for MMP9 -1562 C/T and MMP13-77A/G should be interpreted with caution due to the probability of false-positive reports.