TCHP drives hepatocarcinogenesis through LLPS-mediated AURKA condensation and enables synergistic therapy

Jingshi Li1, Yan Li1, Xilang Pan1

  • 1Precision Research Center for Refractory Diseases, Shanghai Jiao Tong University Pioneer Research Institute for Molecular and Cell Therapies, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, State Key Laboratory of Innovative Immunotherapy, School of Pharmaceutical Sciences, Shanghai Jiao Tong University, Shanghai, China; Department of Pathophysiology, College of Basic Medical Sciences, Shanghai Jiao Tong University, Shanghai, China.

Cell Death & Disease
|April 25, 2026
PubMed

Insights

Trichoplein (TCHP) drives liver cancer by ensuring mitotic fidelity. Inhibiting TCHP or the TCHP-AURKA axis halts tumor growth and sensitizes cancer cells to existing therapies, offering new treatment strategies.

Area of Science:

  • Oncology
  • Cell Biology
  • Molecular Medicine

Background:

  • Liver cancer poses a significant global health burden.
  • Centrosomal protein dysregulation is linked to cancer development.
  • The role of Trichoplein (TCHP) in liver cancer is not well understood.

Purpose of the Study:

  • To investigate the role of TCHP in liver cancer.
  • To explore TCHP as a potential therapeutic target for liver cancer.

Main Methods:

  • Analysis of TCHP expression in human liver cancer tissues.
  • In vivo studies using mouse models of hepatocarcinogenesis.
  • Investigation of TCHP's molecular mechanism involving AURKA.
  • Assessment of TCHP inhibition and combination therapy with alisertib.

Main Results:

  • TCHP is upregulated in hepatocellular carcinoma and hepatoblastoma, correlating with poor survival.
  • TCHP overexpression accelerates liver cancer in mice; TCHP depletion inhibits tumor growth.
  • TCHP promotes liver tumorigenesis by enhancing AURKA activation via phase separation at centrosomes.
  • TCHP inhibition suppresses tumor growth and sensitizes liver cancer cells to alisertib.

Conclusions:

  • TCHP is an oncogenic driver and therapeutic vulnerability in liver cancer.
  • The TCHP-AURKA axis represents a promising target for novel liver cancer therapies.
  • Targeting TCHP offers potential for synergistic treatment strategies with reduced toxicity.

Related Concept Videos

Cirrhosis II: Pathophysiology01:24

Cirrhosis II: Pathophysiology

Cirrhosis is a progressive chronic liver injury caused by prolonged inflammation, excessive fibrotic remodeling, and impaired regeneration. Over time, repeated hepatic insults disrupt the liver’s architecture and function, leading to reduced blood flow, impaired bile drainage, and diminished metabolic capacity.Pathophysiology of cirrhosisCirrhosis arises from three main responses to chronic liver damage: inflammation, immune activation, and hepatocyte death. These processes lead to...
33
Mutagenicity and Carcinogenicity01:25

Mutagenicity and Carcinogenicity

Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
2.0K
DNA Damage can Stall the Cell Cycle02:36

DNA Damage can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
8.5K
DNA Damage Can Stall the Cell Cycle02:36

DNA Damage Can Stall the Cell Cycle

In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
2.3K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
5.1K
Restarting Stalled Replication Forks02:37

Restarting Stalled Replication Forks

DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
5.0K