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Enhanced expression of PKM2 associates with the biological properties of cancer stem cells from A549 human lung cancer cells
Author(s) -
ChangYing Guo,
Yan Chen,
Lan Luo,
Shinji Goto,
Yoshishige Urata,
Jianjun Xu,
Xiaoming Wen,
Yukang Kuang,
Fangfang Tou,
TaoSheng Li
Publication year - 2017
Publication title -
oncology reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.094
H-Index - 96
eISSN - 1791-2431
pISSN - 1021-335X
DOI - 10.3892/or.2017.5438
Subject(s) - pkm2 , cancer stem cell , lung cancer , cancer research , cancer , cd44 , a549 cell , cancer cell , stem cell , biology , pyruvate kinase , medicine , cell , pathology , microbiology and biotechnology , glycolysis , biochemistry , enzyme
Cancer cells express the M2 isoform of glycolytic enzyme pyruvate kinase (PKM2) for favoring the survival under a hypoxic condition. Considering the relative low oxygen microenvironment in stem cell niche, we hypothesized that an enhanced PKM2 expression associates with the biological properties of cancer stem cells. We used A549 human lung cancer cell line and surgical resected lung cancer tissue samples from patients for experiments. We confirmed the co-localization of PKM2 and CD44, a popular marker for cancer stem cells in lung cancer tissue samples from patients. The expression of PKM2 was clearly observed in approximately 80% of the A549 human lung cancer cells. Remarkably, enhanced expression of PKM2 was specially observed in these cells that also positively expressed CD44. Downregulation of PKM2 in CD44+ cancer stem cells by siRNA significantly impaired the potency for spheroid formation, decreased the cell survival under fetal bovine serum deprivation and hypoxic conditions, but increased their sensitivity to anti-cancer drug of cisplatin and γ-ray. The enhanced expression of PKM2 seems to associate with the biological properties of cancer stem cells from A549 human lung cancer cells. Selective targeting of PKM2 may provide a new strategy for cancer therapy, especially for patients with therapeutic resistance.

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