Discovery of Functional Alternatively Spliced PKM Transcripts in Human Cancers

Author:

Li XiangyuORCID,Kim Woonghee,Arif MuhammadORCID,Gao Chunxia,Hober AndreasORCID,Kotol DavidORCID,Strandberg LinnéaORCID,Forsström Björn,Sivertsson ÅsaORCID,Oksvold PerORCID,Turkez Hasan,Grøtli Morten,Sato Yusuke,Kume Haruki,Ogawa Seishi,Boren JanORCID,Nielsen Jens,Uhlen Mathias,Zhang ChengORCID,Mardinoglu AdilORCID

Abstract

Pyruvate kinase muscle type (PKM) is a key enzyme in glycolysis and plays an important oncological role in cancer. However, the association of PKM expression and the survival outcome of patients with different cancers is controversial. We employed systems biology methods to reveal prognostic value and potential biological functions of PKM transcripts in different human cancers. Protein products of transcripts were shown and detected by western blot and mass spectrometry analysis. We focused on different transcripts of PKM and investigated the associations between their mRNA expression and the clinical survival of the patients in 25 different cancers. We find that the transcripts encoding PKM2 and three previously unstudied transcripts, namely ENST00000389093, ENST00000568883, and ENST00000561609, exhibited opposite prognostic indications in different cancers. Moreover, we validated the prognostic effect of these transcripts in an independent kidney cancer cohort. Finally, we revealed that ENST00000389093 and ENST00000568883 possess pyruvate kinase enzymatic activity and may have functional roles in metabolism, cell invasion, and hypoxia response in cancer cells. Our study provided a potential explanation to the controversial prognostic indication of PKM, and could invoke future studies focusing on revealing the biological and oncological roles of these alternative spliced variants of PKM.

Funder

Knut och Alice Wallenbergs Stiftelse

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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