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  Endocytosis-mediated replenishment of amino acids favors cancer cell proliferation and survival in chromophobe renal cell carcinoma

Xiao, Y., Rabien, A., Buschow, R., Amstislavskiy, V., Busch, J., Kilic, E., et al. (2020). Endocytosis-mediated replenishment of amino acids favors cancer cell proliferation and survival in chromophobe renal cell carcinoma. Cancer research: an official organ of the American Association for Cancer Research, 2020. doi:10.1158/0008-5472.CAN-20-1998.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0007-4F87-9 Version Permalink: http://hdl.handle.net/21.11116/0000-0007-4F88-8
Genre: Journal Article

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© 2020, American Association for Cancer Research
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 Creators:
Xiao, Yi1, Author              
Rabien, Anja, Author
Buschow, Rene2, Author              
Amstislavskiy, Vyacheslav3, Author              
Busch, Jonas, Author
Kilic, Ergin, Author
Villegas, Sonia L. , Author
Timmermann, Bernd4, Author              
Schütte, Moritz, Author
Mielke, Thorsten2, Author              
Yaspo, Marie-Laure3, Author              
Jung, Klaus, Author
Meierhofer, David1, Author              
Affiliations:
1Mass Spectrometry (Head: David Meierhofer), Scientific Service (Head: Christoph Krukenkamp), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479669              
2Microscopy and Cryo-Electron Microscopy (Head: Thorsten Mielke), Scientific Service (Head: Christoph Krukenkamp), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479668              
3Gene Regulation and Systems Biology of Cancer (Marie-Laure Yaspo), Independent Junior Research Groups (OWL), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_2117287              
4Sequencing (Head: Bernd Timmermann), Scientific Service (Head: Christoph Krukenkamp), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1479670              

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 Abstract: Chromophobe renal cell carcinoma (chRCC) accounts for approximately 5% of all renal cancers and around 30% of chRCC cases have mutations in TP53. ChRCC is poorly supported by microvessels and has markably lower glucose uptake than clear cell RCC (ccRCC) and papillary RCC (pRCC). Currently, the metabolic status and mechanisms by which this tumor adapts to nutrient-poor microenvironments remain to be investigated. In this study, we performed proteome and metabolome profiling of chRCC tumors and adjacent kidney tissues and identified major metabolic alterations in chRCC tumors, including the classical Warburg effect, the downregulation of gluconeogenesis and amino acid metabolism, and the upregulation of protein degradation and endocytosis. ChRCC cells depended on extracellular macromolecules as an amino acid source by activating endocytosis to sustain cell proliferation and survival. Inhibition of the PLCG2/IP3/Ca2+/PKC pathway significantly impaired the activation of endocytosis for amino acids uptakes into chRCC cells. In chRCC, whole-exome sequencing revealed that TP53 mutations were not related to expression of PLCG2 and activation of endocytosis. Our study provides novel perspectives on metabolic rewiring in chRCC and identifies the PLCG2/IP3/Ca2+/PKC axis as a potential therapeutic target in chRCC patients.

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Language(s): eng - English
 Dates: 2020-10-202020-10-28
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1158/0008-5472.CAN-20-1998
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Title: Cancer research : an official organ of the American Association for Cancer Research
  Other : Cancer Res.
Source Genre: Journal
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Publ. Info: Baltimore, Md. : Waverly Press
Pages: - Volume / Issue: 2020 Sequence Number: - Start / End Page: - Identifier: ISSN: 0008-5472 (print) 1538-7445 (online)
CoNE: https://pure.mpg.de/cone/journals/resource/991042743115962