Tid-1 Interacts with the von Hippel-Lindau Protein and Modulates Angiogenesis by Destabilization of HIF-1α

Author:

Bae Moon-Kyoung12,Jeong Joo-Won1,Kim Se-Hee1,Kim Soo-Young1,Kang Hye Jin1,Kim Dong-Min1,Bae Soo-Kyung3,Yun Il2,Trentin Grace A.4,Rozakis-Adcock Maria4,Kim Kyu-Won1

Affiliation:

1. 1Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, Korea; Colleges of

2. 2Dentistry and

3. 3Medicine, Pusan National University, Busan, Korea; and

4. 4Department of Laboratory Medicine and Pathology, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada

Abstract

Abstract The von Hippel-Lindau protein (pVHL) is a major tumor suppressor protein and also associated with the inhibition of angiogenesis via HIF-1α ubiquitination and proteasomal degradation. To further elucidate the biological activity of pVHL in angiogenesis, pVHL-interacting proteins were screened using the yeast two-hybrid system. We found that a mouse homologue of the long form of Drosophila tumor suppressor l(2)tid, Tid-1L, directly interacts with pVHL in vitro and in vivo. Furthermore, Tid-1L protein; enhanced the interaction between HIF-1α and pVHL, leading to the destabilization of HIF-1α protein; therefore, Tid-1L protein decreased vascular endothelial growth factor expression and inhibited angiogenesis in vivo and in vitro. These findings propose that Tid-1L may play a critical role in pVHL-mediated tumor suppression by modulating the pVHL-dependent HIF-1α stability.

Publisher

American Association for Cancer Research (AACR)

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