Brusatol attenuated proliferation and invasion induced by KRAS in differentiated thyroid cancer through inhibiting Nrf2

IF 3.9 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Journal of Endocrinological Investigation Pub Date : 2023-12-07 DOI:10.1007/s40618-023-02248-4
Z. Gong, L. Xue, A. C. Vlantis, C. A. van Hasselt, J. Y. K. Chan, J. Fang, R. Wang, Y. Yang, D. Li, X. Zeng, M. C. F. Tong, G. G. Chen
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Abstract

Background

Poorly differentiated thyroid cancer (PDTC) and anaplastic thyroid cancer (ATC) can be developed from differentiated thyroid cancer, and this dedifferentiated transformation leads to poor prognosis and high mortality. The role of Nrf2 in the dedifferentiation of differentiated thyroid cancer (DTC) induced by KRAS remains unclear.

Methods and materials

In this study, two DTC cell lines, BCPAP and WRO, were used to evaluate the function of Nrf2 in the dedifferentiation caused by wild-type KRAS (KRAS-WT) and G12V point mutation KRAS (KRAS-G12V).

Results

The overexpression of KRAS-WT and KRAS-G12V increased the proliferative and invasive ability of BCPAP and WRO cells. Aggressive morphology was observed in KRAS-WT and KRAS-G12V overexpressed WRO cells. These results suggested that overexpression of KRAS-WT or KRAS-G12V may induce dedifferentiation in DTC cells. The expression of Nrf2 was increased by KRAS-WT and KRAS-G12V in DTC cells. In addition, compared with normal thyroid tissues, the expression of Nrf2 protein was considerably higher in thyroid cancer tissues on immunohistochemistry (IHC) staining, and the increased expression of Nrf2 indicated a poor prognosis of thyroid cancer. These results indicated that Nrf2 is the KRAS downstream molecule in thyroid cancer. Functional studies showed that the Nrf2 inhibitor Brusatol counteracted the proliferative and invasive abilities induced by KRAS-WT and KRAS-G12V in BCPAP and WRO cells. In addition, the xenograft assay further confirmed that Brusatol inhibits tumor growth induced by KRAS-WT and KRAS-G12V.

Conclusion

Collectively, this study suggests that Nrf2 could be a promising therapeutic target in KRAS-mediated dedifferentiation of thyroid cancer.

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布芦沙托通过抑制 Nrf2 减轻 KRAS 诱导的分化型甲状腺癌增殖和侵袭
背景由分化型甲状腺癌发展而来的甲状腺低分化癌(PDTC)和甲状腺无弹性癌(ATC)可导致不良预后和高死亡率。本研究利用两种DTC细胞系BCPAP和WRO来评估Nrf2在野生型KRAS(KRAS-WT)和G12V点突变KRAS(KRAS-G12V)引起的去分化中的作用。结果 KRAS-WT和KRAS-G12V的过表达增加了BCPAP和WRO细胞的增殖和侵袭能力。在 KRAS-WT 和 KRAS-G12V 过表达的 WRO 细胞中观察到了侵袭性形态。这些结果表明,KRAS-WT或KRAS-G12V的过表达可能会诱导DTC细胞发生去分化。在DTC细胞中,KRAS-WT和KRAS-G12V增加了Nrf2的表达。此外,与正常甲状腺组织相比,免疫组化染色法(IHC)显示甲状腺癌组织中Nrf2蛋白的表达明显升高,Nrf2表达的升高表明甲状腺癌的预后较差。这些结果表明,Nrf2是甲状腺癌中KRAS的下游分子。功能研究表明,Nrf2抑制剂Brusatol能抑制KRAS-WT和KRAS-G12V诱导的BCPAP和WRO细胞的增殖和侵袭能力。此外,异种移植试验进一步证实,Brusatol 能抑制 KRAS-WT 和 KRAS-G12V 诱导的肿瘤生长。
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来源期刊
Journal of Endocrinological Investigation
Journal of Endocrinological Investigation 医学-内分泌学与代谢
CiteScore
8.70
自引率
7.40%
发文量
242
审稿时长
3 months
期刊介绍: The Journal of Endocrinological Investigation is a well-established, e-only endocrine journal founded 36 years ago in 1978. It is the official journal of the Italian Society of Endocrinology (SIE), established in 1964. Other Italian societies in the endocrinology and metabolism field are affiliated to the journal: Italian Society of Andrology and Sexual Medicine, Italian Society of Obesity, Italian Society of Pediatric Endocrinology and Diabetology, Clinical Endocrinologists’ Association, Thyroid Association, Endocrine Surgical Units Association, Italian Society of Pharmacology.
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