4.7 Article Retracted Publication

被撤回的出版物: Quercetin Inhibits Tumorigenesis of Colorectal Cancer Through Downregulation of hsa_circ_0006990 (Retracted article. See vol. 14, 2023)

Journal

FRONTIERS IN PHARMACOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.874696

Keywords

tumor-associated macrophages; quercetin; hsa_circ_0006990-miR-132-3p; miR-342-3p network; autophagy; colorectal cancer

Funding

  1. Traditional Chinese Medicine Clinical Key Specialty Construction Project of Shanghai Putuo District [ptzyzk2101]
  2. Traditional Chinese Medicine Research Project of Shanghai Municipal Commission of Health and Family Planning [2018JP004]
  3. Traditional Chinese Medicine Research Project of Shanghai Municipal Health Commission [2020JP004]
  4. Research Project of Shanghai Putuo District Central Hospital [2020364A]
  5. Clinical Specialized Discipline of Health System of Putuo District in Shanghai [2021tszk01]
  6. Health System Innovation Project of Shanghai Putuo Science and Technology Commission [ptkwws202109, ptkwws202002]

Ask authors/readers for more resources

Quercetin inhibits the tumorigenesis of CRC by inhibiting the polarization of M2 macrophages and downregulating hsa_circ_0006990. This finding provides useful insights for exploring new methods of treating CRC.
Quercetin can significantly inhibit the progression of colorectal cancer (CRC). However, its specific mechanism remains largely unclear. In this study, we aimed to explore the correlation among quercetin, tumour-associated macrophages (TAMs) and circular RNAs (circRNAs) in the progression of CRC and to present a novel strategy for the treatment of CRC. In this study, we revealed that quercetin could suppress the autophagy of M2-TAMs and induced their differentiation into M1-TAMs, by which quercetin significantly reversed the inhibition of M2-TAMS on CRC cell apoptosis and the promotion of M2-TAMS on CRC cell proliferation. Moreover, quercetin could promote the expression of downregulated hsa_circ_0006990 in CRC cells co-cultured with M2-TAMs, and the overexpression of hsa_circ_0006990 significantly reversed the anti-tumour effect of quercetin on CRC. Furthermore, we found quercetin can notably suppress the progression of CRC via mediation of the hsa_circ_0006990/miR-132-3p/MUC13 axis. In conclusion, our results suggested that quercetin inhibits the tumorigenesis of CRC via inhibiting the polarisation of M2 macrophages and downregulating hsa_circ_0006990. Our study provides useful insights for those exploring new methods of treating CRC.

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