Arsenic trioxide targets Hsp60, triggering degradation of p53 and survivin

Author:

Hu Xuqiao1,Li Hongyan1,Ip Tiffany Ka-Yan1,Cheung Yam Fung1,Koohi-Moghadam Mohamad12,Wang Haibo1,Yang Xinming1,Tritton Daniel N.1,Wang Yuchuan1,Wang Yi1ORCID,Wang Runming1,Ng Kwan-Ming13ORCID,Naranmandura Hua4ORCID,Tse Eric Wai-Choi5ORCID,Sun Hongzhe1ORCID

Affiliation:

1. Department of Chemistry and CAS-HKU Joint Laboratory of Metallomics on Health and Environment, The University of Hong Kong, Hong Kong SAR, P. R. China

2. Division of Applied Oral Sciences and Community Dental Care, Faculty of Dentistry, University of Hong Kong, Hong Kong SAR, P. R. China

3. Department of Chemistry, Shantou University, Shantou, Guangdong, 515063, P. R. China

4. Department of Toxicology, School of Medicine and Public Health, Zhejiang University, Hangzhou, P.R. China

5. Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Queen Mary Hospital, Hong Kong, P. R. China

Abstract

A highly selective organoarsenic fluorescent probe As-AC and quantitative proteomics were employed to track arsenic-binding and regulating proteins in live leukemia cells. Hsp60 was validated as a new target of ATO.

Funder

Research Grants Council, University Grants Committee

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

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