Defueling the cancer: ATP synthase as an emerging target in cancer therapy

Ting Wang1,2, Fei Ma3, Hai-Li Qian1

  • 1State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

Insights

Cancer cells reprogram metabolism, often overexpressing mitochondrial ATP synthase (MAS). This enzyme

Area of Science:

  • Biochemistry
  • Oncology
  • Molecular Biology

Background:

  • Reprogramming of cellular metabolism is a hallmark of cancer.
  • Mitochondrial ATP synthase (MAS) is crucial for cellular ATP production.
  • High MAS expression correlates with poor prognosis in multiple cancers, including glioblastoma, ovarian, prostate, breast, and renal cell carcinoma.

Purpose of the Study:

  • To review the role of ATP synthase in cancer.
  • To discuss ATP synthase as a therapeutic target.
  • To summarize recent ATP synthase inhibitors for cancer treatment.

Main Methods:

  • Literature review of studies on ATP synthase in cancer.
  • Analysis of the link between MAS expression and cancer prognosis.
  • Examination of cell surface ATP synthase involvement in tumorigenesis.
  • Review of current ATP synthase inhibitors and their clinical testing.

Main Results:

  • Mitochondrial ATP synthase (MAS) is highly expressed in various cancers, correlating with poor prognosis.
  • Cell surface-localized ATP synthase contributes to angiogenesis, tumorigenesis, and metastasis.
  • ATP synthase inhibitors show potential in suppressing tumor growth.

Conclusions:

  • ATP synthase is a critical enzyme in cancer metabolism and progression.
  • Targeting ATP synthase presents a promising therapeutic strategy for cancer.
  • Ongoing research and clinical trials are evaluating ATP synthase inhibitors for cancer treatment.

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