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Open AccessJournal ArticleDOI

CircRNA_102272 Promotes Cisplatin-Resistance in Hepatocellular Carcinoma by Decreasing MiR-326 Targeting of RUNX2.

TLDR
CircRNA_102272 is significantly increased in HCC tissues and cells and promotes HCC cell proliferation and cisplatin-resistance and acts as a ceRNA to suppress the expression and activity of miR-326, leading to the increase in RUNX2 expression.
Abstract
Background Hepatocellular carcinoma (HCC) is the leading cause of tumor-associated death in males and females worldwide. HCC is mostly diagnosed at advanced stages and the chemotherapeutic cisplatin is one of the major therapeutic options in the treatment of patients with treating advanced HCC. Despite several reports on HCC multidrug resistance, the underlying regulatory mechanisms are still unclear. Methods RT-PCR was performed to detect circRNA_102272, miR-326 and RUNX2 expression. The CCK8 assay was used to examine cell proliferation and cisplatin IC50 values. The luciferase reporter assay was performed to verify complementary combinations between circRNA_102272 and miR-326 and between miR-326 and RUNX2. Results CircRNA_102272 expression was upregulated in HCC tissues and cells. CircRNA_102272 knockdown suppressed HCC cell proliferation and decreased cisplatin-resistance. In addition, circRNA_102272 facilitated HCC cisplatin-resistance by regulating the miR-326/RUNX2 axis. Conclusion CircRNA_102272 is significantly increased in HCC tissues and cells and promotes HCC cell proliferation and cisplatin-resistance. More importantly, circRNA acts as a ceRNA to suppress the expression and activity of miR-326, leading to the increase in RUNX2 expression. By elucidating circRNA_102272 role and mechanism of action in HCC, our study provides insights and an opportunity to overcome cisplatin-resistance in HCC.

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Journal ArticleDOI

Wnt/β-Catenin Signaling as a Driver of Hepatocellular Carcinoma Progression: An Emphasis on Molecular Pathways.

TL;DR: In this article, the role of Wnt signaling in hepatocellular carcinoma (HCC) and its association with progression and therapy response based on pre-clinical and clinical evidence is discussed.
Journal ArticleDOI

circMRPS35 promotes malignant progression and cisplatin resistance in hepatocellular carcinoma

TL;DR: In this paper , the authors identified a functional RNA, hsa_circ_0000384 (circMRPS35), from public tumor databases using a set of computational analyses, and further identified that circMRPS 35 was highly expressed in 35 pairs of HCC from patients.
Journal ArticleDOI

circMRPS35 promotes malignant progression and cisplatin resistance in hepatocellular carcinoma.

TL;DR: In this paper, the authors identified a functional RNA, hsa_circ_0000384 (circMRPS35), from public tumor databases using a set of computational analyses, and further identified that circMRPS 35 was highly expressed in 35 pairs of HCC from patients.
Journal ArticleDOI

Cancer-associated fibroblast exosomes promote chemoresistance to cisplatin in hepatocellular carcinoma through circZFR targeting signal transducers and activators of transcription (STAT3)/ nuclear factor -kappa B (NF-κB) pathway

TL;DR: In vivo tumor xenograft experiments showed that knockdown ofcircZFR inhibited tumor growth and weakened DDP resistance, while CAFs-derived exosomes incubation increased the expression of circZFR, inhibited the STAT3/NF-κB pathway, promoted tumor growth, and enhanced DDP Resistance.
Journal ArticleDOI

The functional roles, cross-talk and clinical implications of m6A modification and circRNA in hepatocellular carcinoma.

TL;DR: In this article, the authors elucidated the biological functions and molecular mechanisms of m6A modification in the carcinogenesis of HCC by illustrating three different regulatory factors ("writer", "eraser", and "reader") of the modification process.
References
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Journal ArticleDOI

Bitter Melon Enhances Natural Killer–Mediated Toxicity against Head and Neck Cancer Cells

TL;DR: It is demonstrated for the first time that BME augments NK-cell–mediated HNSCC killing activity, implicating an immunomodulatory role of BME.
Journal ArticleDOI

LINC00052 regulates the expression of NTRK3 by miR-128 and miR-485-3p to strengthen HCC cells invasion and migration.

TL;DR: It is found that invasion, migration and proliferation abilities in SMMC7721 cell were inhibited after up-expressing LINC00052 and it was identified that NTRK3 was the target gene of L INC00052, a new mechanism for understanding hepatocarcinoma cells invasion and migration.
Journal Article

miR-326 regulates EMT and metastasis of endometrial cancer through targeting TWIST1.

TL;DR: It is demonstrated that miR-326 served as a tumor suppressor by targeting TWIST1, and may serve as a biomarker or therapeutic target for patients with EC.
Journal ArticleDOI

Clinical significance of RUNX2 expression in patients with nonsmall cell lung cancer: a 5-year follow-up study

TL;DR: Examination of expression and prognostic significance of runt-related transcription factor (RUNX)-2 in human nonsmall cell lung cancer showed that RUNX2 may play an important role in NSCLC tumorigenesis, and RUNx2 might serve as a novel prognostic marker in NS CLC.
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