TY - JOUR
T1 - LINC01296 promotes cancer stemness traits in oral carcinomas by sponging miR-143
AU - Liang, Kuang Yuan
AU - Ho, D.C.Y.
AU - Yang, Hsiu Pin
AU - Hsieh, Pei Ling
AU - Fang, Chih Yuan
AU - Tsai, Lo Lin
AU - Chao, Shih Chi
AU - Liu, Chia Ming
AU - Yu, Cheng Chia
N1 - Funding Information:
The administrative and financial supports of this study were from the Kaohsiung Armed Forces General Hospital Gangshan Branch (KAFGH-A-111002), Chung Shan Medical University Hospital (CSH-2021-C-010), Wan Fang Hospital (111-wf-phd-01), and Ministry of Science and Technology (MOST108-2314-B-038-036) in Taiwan.
Publisher Copyright:
© 2023 Association for Dental Sciences of the Republic of China
PY - 2023
Y1 - 2023
N2 - Background/purpose: Emerging evidence has shown that various failures in cancer therapy, such as drug resistance, metastasis, and cancer relapse are attributed to cancer stem cells (CSCs). Also, growing attention has been paid to the regulation of non-coding RNAs in cancer stemness. Here, we aimed to investigate the contribution of LINC01296 in the modulation of oral CSCs. Materials and methods: The phenotypic assays including migration, invasion, and colony-forming abilities were carried out in CSCs of two types of oral cancer cells (SAS and GNM) following the knockdown of LINC01296. In addition, the percentage of cells expressing stemness marker, ALDH1, and drug resistance marker, ABCG2, was examined as well as the self-renewal capacity after silencing of LINC01296. Moreover, a luciferase reporter was used to validate the direct interaction between LINC01296 and miR-143. Results: Our results showed that LINC01296 was significantly overexpressed in oral cancer tissues and positively correlated with stemness markers. The phenotypic and flow cytometry assays demonstrated that suppression of LINC01296 reduced the aggressiveness, cancer stemness features, and colony-forming and self-renewal abilities in oral CSCs. Furthermore, we demonstrated that LINC01296 may enhance cancer stemness features through suppression of the effect of miR-143. Conclusion: Silencing of LINC01296 may be a promising direction for oral cancer therapy by reducing cancer stemness via regulation of miR-143.
AB - Background/purpose: Emerging evidence has shown that various failures in cancer therapy, such as drug resistance, metastasis, and cancer relapse are attributed to cancer stem cells (CSCs). Also, growing attention has been paid to the regulation of non-coding RNAs in cancer stemness. Here, we aimed to investigate the contribution of LINC01296 in the modulation of oral CSCs. Materials and methods: The phenotypic assays including migration, invasion, and colony-forming abilities were carried out in CSCs of two types of oral cancer cells (SAS and GNM) following the knockdown of LINC01296. In addition, the percentage of cells expressing stemness marker, ALDH1, and drug resistance marker, ABCG2, was examined as well as the self-renewal capacity after silencing of LINC01296. Moreover, a luciferase reporter was used to validate the direct interaction between LINC01296 and miR-143. Results: Our results showed that LINC01296 was significantly overexpressed in oral cancer tissues and positively correlated with stemness markers. The phenotypic and flow cytometry assays demonstrated that suppression of LINC01296 reduced the aggressiveness, cancer stemness features, and colony-forming and self-renewal abilities in oral CSCs. Furthermore, we demonstrated that LINC01296 may enhance cancer stemness features through suppression of the effect of miR-143. Conclusion: Silencing of LINC01296 may be a promising direction for oral cancer therapy by reducing cancer stemness via regulation of miR-143.
KW - Cancer stemness
KW - LINC01296
KW - MicroRNA-143
KW - Oral cancer
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U2 - 10.1016/j.jds.2023.01.008
DO - 10.1016/j.jds.2023.01.008
M3 - Article
AN - SCOPUS:85147365766
SN - 1991-7902
JO - Journal of Dental Sciences
JF - Journal of Dental Sciences
ER -