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MicroRNAs as Modulators of Oral Tumorigenesis—A Focused Review

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TLDR
In this paper, the role of microRNAs in regulating various hallmarks of oral tumorigenesis is discussed, including sustaining proliferative signaling, evading growth suppressors, resisting cell death activating invasion and metastasis, and inducing angiogenesis.
Abstract
Oral cancers constitute the majority of head and neck tumors, with a relatively high incidence and poor survival rate in developing countries. While the five-year survival rates of the oral cancer patients have increased to 65%, the overall survival for advanced stages has been at 27% for the past ten years, emphasizing the necessity for further understanding the etiology of the disease, diagnosis, and formulating possible novel treatment regimens. MicroRNAs (miRNAs), a family of small non-coding RNA, have emerged as master modulators of gene expression in various cellular and biological process. Aberrant expression of these dynamic molecules has been associated with many human diseases, including oral cancers. The deregulated miRNAs have been shown to control various oncogenic processes, including sustaining proliferative signaling, evading growth suppressors, resisting cell death activating invasion and metastasis, and inducing angiogenesis. Hence, the aberrant expression of miRNAs associated with oral cancers, makes them potential candidates for the investigation of functional markers, which will aid in the differential diagnosis, prognosis, and development of novel therapeutic regimens. This review presents a holistic insight into our understanding of the role of miRNAs in regulating various hallmarks of oral tumorigenesis.

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miRNAs in Cancer (Review of Literature)

TL;DR: The current knowledge about the possibility of using miRNA as a diagnostic marker and a potential target in modern anticancer therapies is discussed.
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Long noncoding RNAs in triple-negative breast cancer: A new frontier in the regulation of tumorigenesis.

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References
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Journal ArticleDOI

Exosomes containing miR-21 transfer the characteristic of cisplatin resistance by targeting PTEN and PDCD4 in oral squamous cell carcinoma.

TL;DR: Exosomes derived from cisplatin-resistant OSCC cells were found to enhance the chemoresistance of OSCC cell and decrease the DNA damage signaling in response to cisPlatin.
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Recent progress in microRNA-based delivery systems for the treatment of human disease

TL;DR: Some representative advances related to the application of viral- and nonviral-mediated miRNA delivery systems are discussed and a new perspective on the future of miRNA-based therapeutic strategies is provided.
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MiR-133a-3p Inhibits Oral Squamous Cell Carcinoma (OSCC) Proliferation and Invasion by Suppressing COL1A1.

TL;DR: Investigation of the effects of miR‐133a‐3p on human oral squamous cell carcinoma (OSCC) cells by regulating gene COL1A1 found it could inhibit the proliferation and migration of OSCC cells through directly targeting COL 1A1 and reducing its expression.
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MiR-145 inhibits oral squamous cell carcinoma (OSCC) cell growth by targeting c-Myc and Cdk6

TL;DR: The data suggest that miR-145 exerts its tumor suppressor function by targeting c-Myc and Cdk6, leading to the inhibition of OSCC cell growth, and may be a rational for diagnostic and therapeutic applications in OSCC.
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