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TTN-AS1 as a potential diagnostic and prognostic biomarker for multiple cancers. | LitMetric

TTN-AS1 as a potential diagnostic and prognostic biomarker for multiple cancers.

Biomed Pharmacother

State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China. Electronic address:

Published: March 2021

AI Article Synopsis

  • Long noncoding RNAs (lncRNAs) are RNA molecules longer than 200 nucleotides that play key roles in biological processes like cell differentiation and the cell cycle.
  • Aberrantly regulated lncRNAs, such as TTN-AS1, can act as oncogenes or tumor suppressors, influencing cancer development and progression.
  • TTN-AS1 is linked to poor prognosis in multiple cancer types, with higher levels correlating to more severe disease, and recent studies focus on its regulatory mechanisms and impact on tumor behavior.

Article Abstract

The long noncoding RNAs (lncRNAs) are non-coding RNAs that are more than 200 nucleotides in length, and one of several types of non-coding RNAs (ncRNAs). The lncRNAs function in diverse biological processes in normal cells, such as cellular differentiation and cell cycle regulation. There is also evidence that some aberrantly regulated lncRNAs function as oncogenes or tumor suppressor genes in various cancers. For example, TTN-AS1 is a lncRNA that binds to titin mRNA (TTN) and has pro-oncogenic effects in many cancers. Overexpression of TTN-AS1 correlates with poor prognosis in breast cancer, lung cancer, digestive system neoplasms, reproductive system cancers, and other cancers. Furthermore, increased TTN-AS1 expression correlates with more advanced pathology and tumor malignancy. In this review, we comprehensively summarize recent studies on the molecular mechanisms of TTN-AS1 regulation and the role of TTN-AS1 in the carcinogenesis and progression of numerous tumors.

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Source
http://dx.doi.org/10.1016/j.biopha.2020.111169DOI Listing

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