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Cited by 239

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Novel insights on m6A RNA methylation in tumorigenesis: a double-edged sword

Open access
Wang, Shaoyun, Chai, Peiwei, Jia, Ruobing, Jia, Renbing·2018·Molecular Cancer

Abstract

N6-methyladenosine (m 6 A), the most prevalent modification of mammalian RNA, has received increasing attention. Although m 6 A has been shown to be associated with biological activities, such as spermatogenesis modulation, cell spermatogenesis and pluripotency, Drosophila sex determination, and the control of T cell homeostasis and response to heat shock, little is known about its roles in cancer biology and cancer stem cells. Recent articles have noted that some genes have abnormal m 6 A expression after tumorigenesis, including genes ABS2, RARA, MYB, MYC, ADAM19 and FOX1 . Abnormal changes in the m 6 A levels of these genes are closely related to tumour occurrence and development. In this review, we summarized the ‘dual edge weapon’ role of RNA methylation in the tumorigenesis. We discussed RNA methylation could lead to not only tumour progression but also tumour suppression. Moreover, we clarified that the abnormal changes in the m 6 A enrichment of specific loci contribute to tumour occurrence and development, thereby representing a novel anti-cancer strategy by restoration to balanced RNA methylation in tumour cells.

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Metadata

Authors
Wang, S., Chai, P., Jia, R., & Jia, R.
Venue
Molecular Cancer
Published
2018-07-21
Volume
17
Issue
1
Pages
101-101
ISSN
1476-4598 (ISSN-L)
OpenAlex
W2883872430
Cited by
239
References
9
FWCI
12.01
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Novel insights on m6A RNA methylation in tumorigenesis: a double-edged sword. https://app.cochat.ai/papers/10.1186/s12943-018-0847-4
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Wang, S., Chai, P., Jia, R., & Jia, R. (2018). Novel insights on m6A RNA methylation in tumorigenesis: a double-edged sword. Molecular Cancer. https://doi.org/10.1186/s12943-018-0847-4

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