» Articles » PMID: 24884829

Changes in PKM2 Associate with Prostate Cancer Progression

Overview
Journal Cancer Invest
Specialty Oncology
Date 2014 Jun 3
PMID 24884829
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Pyruvate kinase M2 (PKM2) is essential for aerobic glycolysis, the dominant metabolic pathway utilized by cancer cells. To determine the association of PKM2 with prostate cancer (PC), we examined 29 primary PC and three lymph node metastatic tumors; elevation of PKM2 was observed in Gleason 8-10 tumors compared to Gleason 6-7 carcinomas. High PKM2 was detected by immunohistochemistry in more aggressive xenograft tumors derived from PC stem-like cells (PCSCs) compared to those produced from non-PCSCs. While PCSCs and non-PCSCs expressed comparable levels of PKM2, distinct posttranslational modifications were observed. Collectively, upregulation and specific modification to PKM2 associate with PC progression.

Citing Articles

Bibliometric analysis of glycolysis and prostate cancer research from 2004 to 2024.

Zhu C, Yang J, Liu L, Li B, Sun T, Sheng W Discov Oncol. 2025; 16(1):34.

PMID: 39800812 PMC: 11725561. DOI: 10.1007/s12672-025-01790-2.


The expression of PKM1 and PKM2 in developing, benign, and cancerous prostatic tissues.

Li L, Cheng S, Yeh Y, Shi Y, Henderson N, Price D Front Oncol. 2024; 14:1392085.

PMID: 38680860 PMC: 11045992. DOI: 10.3389/fonc.2024.1392085.


The expression of PKM1 and PKM2 in developing, benign, and cancerous prostatic tissues.

Li L, Cheng S, Yeh Y, Shi Y, Henderson N, Price D bioRxiv. 2024; .

PMID: 38260443 PMC: 10802256. DOI: 10.1101/2023.09.27.559832.


Phytochemicals targeting glycolysis in colorectal cancer therapy: effects and mechanisms of action.

Zhan L, Su F, Li Q, Wen Y, Wei F, He Z Front Pharmacol. 2023; 14:1257450.

PMID: 37693915 PMC: 10484417. DOI: 10.3389/fphar.2023.1257450.


A Practical and Analytical Comparative Study of Gel-Based Top-Down and Gel-Free Bottom-Up Proteomics Including Unbiased Proteoform Detection.

Ercan H, Resch U, Hsu F, Mitulovic G, Bileck A, Gerner C Cells. 2023; 12(5).

PMID: 36899884 PMC: 10000902. DOI: 10.3390/cells12050747.