Inhibition of NPC1 suppresses cell proliferation and β-catenin signaling activation of liver cancer

Niemann-Pick Type C1 (NPC1) plays a significant role in the development of liver diseases and liver cancer. Our objective was to investigate the involvement of NPC1 in regulating liver cancer development. We observed that high levels of NPC1 expression in tumor tissues from patients with liver cancer were associated with a poor prognosis. Through in vitro experiments, we found that inhibiting NPC1 expression reduced the proliferation, invasion, and migration of liver cancer cells, while also inducing apoptosis in these cells. Additionally, the inhibition of NPC1 led to decreased activation of Wnt/β-catenin signaling. In vivo studies further supported our findings by demonstrating that the suppression of liver cancer cell growth was effectively achieved through the inhibition of NPC1. Overall, our results strongly indicate that the inhibition of NPC1 suppresses liver cancer cell proliferation. Targeting NPC1 is a promising potential therapeutic strategy for liver cancer.

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Publication Details

Journal
Journal of Cancer Research and Clinical Oncology
Published
2024-11-15
DOI
https://doi.org/10.1007/s00432-024-06023-7
Citations
2
Primary Topic
Cancer-related gene regulation
Type
article
Field-Weighted Citation Impact
0.47

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article

Inhibition of NPC1 suppresses cell proliferation and β-catenin signaling activation of liver cancer

Hong Tang, Min He, Han Chen, Ning Han et al.
2 citations
Journal of Cancer Research and Clinical Oncology
Cancer-related gene regulation
0.47
article

Inhibition of NPC1 suppresses cell proliferation and β-catenin signaling activation of liver cancer

Hong Tang, Min He, Han Chen, Ning Han, Dan Cao
article en
2 citations

Abstract

Niemann-Pick Type C1 (NPC1) plays a significant role in the development of liver diseases and liver cancer. Our objective was to investigate the involvement of NPC1 in regulating liver cancer development. We observed that high levels of NPC1 expression in tumor tissues from patients with liver cancer were associated with a poor prognosis. Through in vitro experiments, we found that inhibiting NPC1 expression reduced the proliferation, invasion, and migration of liver cancer cells, while also inducing apoptosis in these cells. Additionally, the inhibition of NPC1 led to decreased activation of Wnt/β-catenin signaling. In vivo studies further supported our findings by demonstrating that the suppression of liver cancer cell growth was effectively achieved through the inhibition of NPC1. Overall, our results strongly indicate that the inhibition of NPC1 suppresses liver cancer cell proliferation. Targeting NPC1 is a promising potential therapeutic strategy for liver cancer.

Journal of Cancer Research and Clinical OncologyVol. 150(11)
Sichuan University (CN), West China Hospital of Sichuan University (CN), Affiliated Hospital of North Sichuan Medical College (CN)
Sichuan University, National Key Research and Development Program of China, West China Hospital, Sichuan University
Good health and well-being
Openalex Percentile: Top 34%
Cancer-related gene regulation
0.47
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