Quantitative assessment of CD44 genetic variants and cancer susceptibility in Asians: a meta-analysis

CD44 is a well-established cancer stem cell marker playing a crucial role in tumor metastasis, recurrence and chemo-resistance. Genetic variants of CD44 have been shown to be associated with susceptibility to various cancers; however, the results are confounding. Hence, we performed a meta-analysis to clarify these associations more accurately. Overall, rs13347 (T vs. C: OR=1.30, p=<0.004, p(corr)=0.032; CT vs. CC: OR=1.29, p=0.015, p(corr)=0.047; TT vs. CC: OR=1.77, p=<0.000, p(corr)=0.018; CT+TT vs. CC: OR=1.34, p=<0.009, p(corr)=0.041) and rs187115 (GG vs. AA: OR=2.34, p=<0.000, p(corr)=0.025; AG vs. AA: OR=1.59, p=<0.000, p(corr)=0.038; G vs. A allele OR=1.56, p=0.000, p(corr)=0.05; AG+GG vs. AA: OR=1.63, p=<0.000, p(corr)=0.013) polymorphisms were found to significantly increase the cancer risk in Asians. On the other hand, rs11821102 was found to confer low risk (A vs. G: OR=0.87, p=<0.027, p(corr)=0.04; AG vs. GG: OR=0.85, p=<0.017, p(corr)=0.01; AG+AA vs. GG: OR=0.86, p=<0.020, p(corr)=0.02). Based on our analysis, we suggest significant role of CD44 variants (rs13347, rs187115 and rs11821102) in modulating individual's cancer susceptibility in Asians. Therefore, these variants may be used as predictive genetic biomarkers for cancer predisposition in Asian populations. However, more comprehensive studies involving other cancers and/or populations, haplotypes, gene-gene and gene-environment interactions are necessary to delineate the role of these variants in conferring cancer risk.