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• W2972917811 abstract "The N6-Methyladenosine (m6A) modification plays an important role in many biological processes, especially tumor development. However, little is still known about how it affects colorectal cancer (CRC) carcinogenesis. Here, we first systematically investigate the association of variants related to m6A modification with the CRC risk in 1,062 CRC cases and 2,184 controls by using our exome-wide association data and followed by two replication sets including 7,341 CRC cases and 7,902 controls. The variant rs8100241 located in ANKLE1 was significantly associated with CRC risk (odds ratio = 0.88, 95% confidence interval = 0.84–0.92, p = 4.85 × 10−8) in 8,403 cases and 10,086 controls. This variant was previously identified to be associated with the susceptibility of breast cancer with BRCA1 mutation triple negative breast cancer. Further functional analysis indicated that overexpression of the rs8100241[A] allele significantly increased the ANKLE1 m6A level and facilitated the ANKLE1 protein expression compared to that of rs8100241[G] allele. We further found the ANKLE1 m6A modification was catalyzed by the “writer” complex (METTL3, METTL14, or WTAP) and recognized by the “reader” YTHDF1. Mechanistically, we found that the ANKLE1 functions as a potential tumor suppressor that inhibits cell proliferation and facilitates the genomic stability. An elevated frequency of micronucleated cells, increased cell proliferation, and colony formation ability were observed when ANKLE1 knockdown. Our study illustrated that the germline missense variant can increase CRC risk by influencing ANKLE1 m6A level, highlighting a clinical potential of variants-associated m6A modification as a risk marker for CRC prevention." @default.
• W2972917811 created "2019-09-19" @default.
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• W2972917811 date "2019-11-06" @default.
• W2972917811 modified "2023-10-17" @default.
• W2972917811 title "<i>ANKLE1</i>N⁶‐Methyladenosine‐related variant is associated with colorectal cancer risk by maintaining the genomic stability" @default.
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• W2972917811 doi "https://doi.org/10.1002/ijc.32677" @default.
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