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Published on: May 30, 2025
Emerging role of non-coding RNAs in the regulation of KRAS
Soudeh Ghafouri-Fard1, Zeinab Shirvani-Farsani2, Bashdar Mahmud Hussen3
1Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
The Kirsten ras oncogene KRAS is a member of the small GTPase superfamily participating in the RAS/MAPK pathway. A single amino acid substitution in KRAS gene has been shown to activate the encoded protein resulting in cell transformation. This oncogene is involved in the malignant transformation in several tissues. Notably, numerous non-coding RNAs have been found to interact with KRAS protein. Such interaction results in a wide array of human disorders, particularly cancers. Orilnc1, KIMAT1, SLCO4A1-AS1, LINC01420, KRAS1P, YWHAE, PART1, MALAT1, PCAT-1, lncRNA-NUTF2P3-001 and TP53TG1 are long non-coding RNAs (lncRNAs) whose interactions with KRAS have been verified in the context of cancer. miR-143, miR-96, miR-134 and miR-126 have also been shown to interact with KRAS in different tissues. Finally, circITGA7, circ_GLG1, circFNTA and circ-MEMO1 are examples of circular RNAs (circRNAs) that interact with KRAS. In this review, we describe the interaction between KRAS and lncRNAs, miRNAs and circRNAs, particularly in the context of cancer.
Insights
The Kirsten ras oncogene (KRAS) interacts with various non-coding RNAs, including long non-coding RNAs (lncRNAs), microRNAs (miRNAs), and circular RNAs (circRNAs). These interactions are significant in understanding and potentially treating various cancers.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- The Kirsten ras oncogene (KRAS) is a key regulator in the RAS/MAPK pathway, crucial for cell signaling.
- Aberrant KRAS activation, often due to mutations, drives cell transformation and is implicated in numerous cancers.
Purpose of the Study:
- To review the interactions between KRAS and different classes of non-coding RNAs.
- To highlight the role of these interactions in cancer development and progression.
Main Methods:
- Literature review of studies investigating KRAS interactions with non-coding RNAs.
- Categorization of interacting non-coding RNAs into long non-coding RNAs (lncRNAs), microRNAs (miRNAs), and circular RNAs (circRNAs).
Main Results:
- Numerous lncRNAs, including MALAT1 and PCAT-1, have verified interactions with KRAS in cancer.
- Specific miRNAs like miR-143 and miR-126 interact with KRAS.
- Several circRNAs, such as circITGA7 and circFNTA, also demonstrate interactions with KRAS.
Conclusions:
- Non-coding RNAs represent a significant layer of KRAS regulation.
- Understanding these KRAS-non-coding RNA interactions is vital for advancing cancer diagnostics and therapeutics.
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