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Updated: Nov 5, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Curcumin suppresses renal carcinoma tumorigenesis by regulating circ-FNDC3B/miR-138-5p/IGF2 axis
Li Xue1, Yuhua Tao2, Yanjuan Yuan3
1Departments of Nephrology.
Abstract:
Curcumin has a vital role in the development of renal carcinoma. Nevertheless, the mechanism of curcumin in renal carcinoma tumorigenesis remains largely unknown. Thirty renal carcinoma patients were recruited. Renal carcinoma cell lines CAKI-1 and ACHN were exposed to curcumin. The levels of circular RNA fibronectin type III domain-containing protein 3B (circ-FNDC3B), microRNA (miR)-138-5p and insulin-like growth factor 2 (IGF2) were detected via quantitative reverse transcription PCR or western blot. Cell proliferation and apoptosis were investigated via 3-(4, 5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2-H-tetrazolium bromide, colony formation analysis, flow cytometry and western blot. Target association between miR-138-5p and circ-FNDC3B or IGF2 was analyzed via dual-luciferase reporter analysis. The function of curcumin in vivo was assessed via a xenograft model. circ-FNDC3B level was enhanced and miR-138-5p abundance was declined in renal carcinoma tissues and cells. Curcumin restrained renal carcinoma cell proliferation and promoted apoptosis. circ-FNDC3B overexpression or miR-138-5p knockdown weakened the influence of curcumin. circ-FNDC3B knockdown hindered cell proliferation and promoted apoptosis by increasing miR-138-5p. IGF2 was targeted via miR-138-5p and positively regulated via circ-FNDC3B. Curcumin decreased xenograft tumor growth via reducing circ-FNDC3B in vivo. Curcumin suppressed renal carcinoma tumorigenesis in vitro and in vivo via regulating circ-FNDC3B/miR-138-5p/IGF2 axis, proposing new insight into renal carcinoma tumorigenesis.
Insights
Curcumin inhibits renal carcinoma by downregulating circ-FNDC3B and upregulating miR-138-5p, impacting the IGF2 pathway. This study reveals curcumin
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Renal carcinoma (kidney cancer) is a significant health concern.
- The precise mechanisms by which curcumin affects renal carcinoma tumorigenesis are not fully understood.
- Circular RNAs (circRNAs) and microRNAs (miRNAs) are increasingly recognized for their roles in cancer development.
Purpose of the Study:
- To elucidate the mechanism of curcumin's action in renal carcinoma.
- To investigate the roles of circ-FNDC3B, miR-138-5p, and IGF2 in renal carcinoma.
- To explore the therapeutic potential of curcumin in renal carcinoma.
Main Methods:
- Quantitative reverse transcription PCR and Western blot to measure molecular levels.
- Cell proliferation and apoptosis assays (MTT, colony formation, flow cytometry).
- Dual-luciferase reporter assays to confirm molecular interactions.
- In vivo xenograft model to assess anti-tumor effects.
Main Results:
- Elevated circ-FNDC3B and decreased miR-138-5p were observed in renal carcinoma tissues and cells.
- Curcumin suppressed renal carcinoma cell proliferation and induced apoptosis.
- Circ-FNDC3B and miR-138-5p modulated curcumin's effects; circ-FNDC3B knockdown promoted apoptosis via miR-138-5p.
- IGF2 was identified as a target of miR-138-5p and positively regulated by circ-FNDC3B.
- Curcumin reduced tumor growth in vivo by decreasing circ-FNDC3B.
Conclusions:
- Curcumin suppresses renal carcinoma tumorigenesis through the circ-FNDC3B/miR-138-5p/IGF2 axis.
- This pathway offers novel insights into renal carcinoma development and potential therapeutic strategies.
- Circ-FNDC3B and miR-138-5p are key mediators of curcumin's anti-cancer effects in renal carcinoma.
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