Glyoxalase 1 and protein kinase C[lambda] as potential therapeutic targets for late-stage breast cancer

Cancer cells upregulate the expression levels of glycolytic enzymes in order to reach the increased glycolysis required. One such upregulated glycolytic enzyme is glyoxalase 1 (GLO 1), which catalyzes the conversion of toxic methylglyoxal to nontoxic S-D-lactoylglutathione. Protein kinase C[lambda]...

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Veröffentlicht in:Oncology letters 2021-07, Vol.22 (1), p.1
Hauptverfasser: Motomura, Hitomi, Ozaki, Ayaka, Tamori, Shoma, Onaga, Chotaro, Nozaki, Yuka, Waki, Yuko, Takasawa, Ryoko, Yoshizawa, Kazumi, Mano, Yasunari, Sato, Tsugumichi, Sasaki, Kazunori, Ishiguro, Hitoshi, Miyagi, Yohei, Nagashima, Yoji, Yamamoto, Kouji, Sato, Keiko, Hanawa, Takehisa, Tanuma, Sei-Ichi, Ohno, Shigeo, Akimoto, Kazunori
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Sprache:eng
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Zusammenfassung:Cancer cells upregulate the expression levels of glycolytic enzymes in order to reach the increased glycolysis required. One such upregulated glycolytic enzyme is glyoxalase 1 (GLO 1), which catalyzes the conversion of toxic methylglyoxal to nontoxic S-D-lactoylglutathione. Protein kinase C[lambda] (PKC[lambda]) is also upregulated in various types of cancer and is involved in cancer progression. In the present study, the association between enhanced glycolysis and PKC[lambda] in breast cancer was investigated. In human breast cancer, high GLO 1 expression was associated with high PKC[lambda] expression at the protein (P
ISSN:1792-1074
DOI:10.3892/ol.2021.12808