Terpenoids from quinoa reverse drug resistance of colon cancer by upregulating miR-495-3p

被引:4
|
作者
Feng, Mangmang [1 ]
Fan, Xiaxia [1 ]
Shi, Jiangying [1 ]
Shan, Shuhua [1 ]
Li, Songtao [1 ]
He, Shuiling [1 ]
Ding, Man [2 ]
Li, Zhuoyu [1 ]
机构
[1] Shanxi Univ, Inst Biotechnol, Key Lab Chem Biol & Mol Engn, Minist Educ, Taiyuan 030006, Peoples R China
[2] Shanxi Univ, Sch Life Sci, Taiyuan, Peoples R China
基金
中国国家自然科学基金;
关键词
quinoa; terpenoids; drug resistance; colon cancer; miR-495-3p; MULTIDRUG-RESISTANCE; P-GLYCOPROTEIN; TRANSPORTERS; EXPRESSION; CELLS; GP;
D O I
10.1002/jsfa.13718
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUND: Quinoa contains far more nutrients than any traditional grain crop. It is known that terpenoids in quinoa have anti-inflammatory and antitumor effects, but their role in reversing drug resistance remains unclear. RESULTS: Our previous studies showed that quinoa-derived terpenoid compounds (QBT) can inhibit the occurrence and development of colon cancer. This study further indicates that QBT markedly reverse drug resistance of colon cancer. The results showed that QBT combined with 5-fluorouracil (5-Fu) treatment significantly enhanced the chemotherapy sensitivity of HCT-8/Fu, compared with 5-Fu treatment alone. Moreover, we found that QBT significantly reduced the expression of drug-resistant proteins (P-gp, MRP1, BCRP), and increased the accumulation of chemotherapy drugs. Taking P-gp as the target for biogenesis prediction analysis, results showed that upregulation of miR-495-3p enhanced the chemosensitivity of drug-resistant HCT-8/Fu cells. Besides, the results showed that miR-495-3p was abnormally methylated in HCT-8/Fu compared with HCT-8 colon cancer cells. The expression of methyltransferases DNMT1, DNMT3a and DNMT3b was abnormal. After QBT treatment, the expression level of methyltransferases returned to normal. In addition, the QBT + 5Fu group showed inhibition of tumors in nude mice. CONCLUSION: QBT treatment downregulated the expression of drug-resistant protein P-gp by inhibiting the methylation of miR-495-3p, and enhanced the accumulation of 5-Fu in vivo, which in turn reversed its chemoresistance. This suggests that QBT has potential ability as a new drug-resistance reversal agent in colorectal cancer. (c) 2024 Society of Chemical Industry.
引用
收藏
页码:8916 / 8927
页数:12
相关论文
共 50 条
  • [31] Circ_0114428 Regulates Sepsis-Induced Kidney Injury by Targeting the miR-495-3p/CRBN Axis
    Yan He
    Yuanzhu Sun
    Jun Peng
    Inflammation, 2021, 44 : 1464 - 1477
  • [32] circTLK1 facilitates the proliferation and metastasis of renal cell carcinoma by regulating miR-495-3p/CBL axis
    Lei, Xiangli
    Yang, Meiling
    Xiao, Zhifang
    Zhang, Heng
    Tan, Shuai
    OPEN LIFE SCIENCES, 2021, 16 (01): : 362 - 374
  • [33] SATB1 3′-UTR and lncRNA-UCA1 competitively bind to miR-495-3p and together regulate the proliferation and invasion of gastric cancer
    Sun, Li
    Liu, Lina
    Yang, Junshu
    Li, Hai
    Zhang, Can
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (04) : 6671 - 6682
  • [34] Downregulated miR-585-3p promotes cell growth and proliferation in colon cancer by upregulating PSME3
    Liu, Chunmei
    Yang, Juan
    Wu, Han
    Li, Jun
    ONCOTARGETS AND THERAPY, 2019, 12 : 6525 - 6534
  • [35] miR-495-3p、miR-181d-5p在宫颈癌患者中的表达及临床意义
    安国静
    赵丹丹
    仝亚坤
    李静
    李敏
    杜巍
    姚文娟
    现代中西医结合杂志, 2024, 33 (04) : 499 - 503
  • [36] The long noncoding RNA LUCAT1 regulates endometrial receptivity via the miR-495-3p/S100P axis
    Shang, Junyu
    Chen, Yumei
    Jiang, Qianwen
    Li, Wenxin
    Lu, Minjun
    Zhou, Jiamin
    Lin, Li
    Xing, Jie
    Zhang, Mengxue
    Zhao, Shijie
    Lu, Jingjing
    Shi, Xuyan
    Liu, Yueqin
    Zhu, Xiaolan
    COMMUNICATIONS BIOLOGY, 2025, 8 (01)
  • [37] The lncRNA GATA3-AS1/miR-495-3p/CENPU axis predicts poor prognosis of breast cancer via the PLK1 signaling pathway
    Lin, Shuangyan
    Zhao, Mingyuan
    Lv, Yanbo
    Mao, Genxiang
    Ding, Shiping
    Peng, Fang
    AGING-US, 2021, 13 (10): : 13663 - 13679
  • [38] miR-495-3p regulates sphingolipid metabolic reprogramming to induce Sphk1/ceramide mediated mitophagy and apoptosis in NSCLC
    Arora, Shweta
    Singh, Prithvi
    Tabassum, Gulnaz
    Dohare, Ravins
    Syed, Mansoor Ali
    FREE RADICAL BIOLOGY AND MEDICINE, 2022, 189 : 71 - 84
  • [39] 血清miR-124-3p和miR-495-3p水平在脓毒症严重程度和急性肾损伤评估中的作用
    尹烨
    张红
    褚一鸣
    陆天明
    国际检验医学杂志, 2024, 45 (11) : 1404 - 1408
  • [40] Circ_0000215 Increases the Expression of CXCR2 and Promoted the Progression of Glioma Cells by Sponging miR-495-3p
    Mutalifu, Nurehemaiti
    Du, Peng
    Zhang, Jingjing
    Akbar, Halik
    Yan, Baofeng
    Alimu, Sulaiman
    Tong, Lingxiao
    Luan, Xinping
    TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2020, 19