Biomedicine & Pharmacotherapy (Apr 2024)

Inhibition of PTPRE suppresses tumor progression and improves sorafenib response in hepatocellular carcinoma

  • Renshun Dong,
  • Tianci Wang,
  • Wei Dong,
  • He Zhu,
  • Qiumeng Liu,
  • Huifang Liang,
  • Xiaoping Chen,
  • Bixiang Zhang,
  • Xuewu Zhang

Journal volume & issue
Vol. 173
p. 116366

Abstract

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Hepatocellular carcinoma (HCC) has a poor prognosis, and the efficacy of current therapeutic strategies is extremely limited in advanced diseases. Our previous study reported that protein tyrosine phosphatase receptor epsilon (PTPRE) is a promoting factor in HCC progression. In this study, our objective was to evaluate the treatment effect of PTPRE inhibitors in different HCC preclinical models. Our results indicated that the PTPRE inhibitory compound 63 (Cpd-63) inhibited tumor cell proliferation, migration, and HCC organoid growth. Mechanism research revealed that Cpd-63 could inhibit the expression of MYC and MYC targets by inhibiting the activation of SRC. Additionally, we found that Cpd-63 could improve the response of sorafenib in HCC cells. In conclusion, we demonstrated that the PTPRE inhibitors represented a potential therapeutic agent for HCC management.

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