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Review

Role of non-coding RNAs as new therapeutic targets in regulating the EMT and apoptosis in metastatic gastric and colorectal cancers

, , , , , , , , , & show all
Pages 2302-2323 | Received 08 Jun 2022, Accepted 01 Aug 2023, Published online: 27 Nov 2023
 

ABSTRACT

Colorectal cancer (CRC) and gastric cancer (GC), are the two most common cancers of the gastrointestinal tract, and are serious health concerns worldwide. The discovery of more effective biomarkers for early diagnosis, and improved patient prognosis is important. Non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), can regulate cellular processes such as apoptosis and the epithelial-mesenchymal transition (EMT) leading to progression and resistance of GC and CRC tumors. Moreover these pathways (apoptosis and EMT) may serve as therapeutic targets, to prevent metastasis, and to overcome drug resistance. A subgroup of ncRNAs is common to both GC and CRC tumors, suggesting that they might be used as biomarkers or therapeutic targets. In this review, we highlight some ncRNAs that can regulate EMT and apoptosis as two opposite mechanisms in cancer progression and metastasis in GC and CRC. A better understanding of the biological role of ncRNAs could open up new avenues for the development of personalized treatment plans for GC and CRC patients.

GRAPHICAL ABSTRACT

Acknowledgements

The authors would like to thank all of those whose fruitful research has contributed in any way to the elucidation of lncRNAs and their activity in cancers.

Authors’ contributions

NE & AH designed the review paper and wrote the manuscript, FB, and SS, and MSM contributed to writing the manuscript and preparing figures, RK, KF, and FRT contributed to revision, MRH, and ARA reviewed and revised the final version of the manuscript and supervised the study.

Availability of data and material

Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

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