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GLO 1 and PKCλ Regulate ALDH1-positive Breast Cancer Stem Cell Survival.
Motomura, Hitomi; Tamori, Shoma; Yatani, Masa-Aki; Namiki, Ayano; Onaga, Chotaro; Ozaki, Ayaka; Takasawa, Ryoko; Mano, Yasunari; Sato, Tsugumichi; Hara, Yasushi; Sato, Keiko; Xiong, Yuyun; Harada, Yohsuke; Hanawa, Takehisa; Tanuma, Sei-Ichi; Sasaki, Kazunori; Ohno, Shigeo; Akimoto, Kazunori.
Afiliación
  • Motomura H; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Tamori S; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Yatani MA; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Namiki A; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Onaga C; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Ozaki A; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Takasawa R; Department of Pharmacy, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Mano Y; Department of Pharmacy, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Sato T; Department of Pharmacy, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Hara Y; Research Institute for Biomedical Sciences, Tokyo University of Science, Chiba, Japan.
  • Sato K; Department of Information Sciences, Faculty of Sciences and Technology, Tokyo University of Science, Chiba, Japan.
  • Xiong Y; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Harada Y; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Hanawa T; Department of Pharmacy, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
  • Tanuma SI; Department of Genomic Medicinal Science, Research Institute for Science and Technology, Organization for Research Advancement, Tokyo University of Science, Chiba, Japan.
  • Sasaki K; Department of Cancer Biology, Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan.
  • Ohno S; Department of Cancer Biology, Institute for Diseases of Old Age, Juntendo University School of Medicine, Tokyo, Japan.
  • Akimoto K; Department of Medicinal and Life Sciences, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan; akimoto@rs.tus.ac.jp.
Anticancer Res ; 41(12): 5959-5971, 2021 Dec.
Article en En | MEDLINE | ID: mdl-34848450
ABSTRACT
BACKGROUND/

AIM:

We examined the inhibitory effects of both glyoxalase 1 (GLO 1) and protein kinase C (PKC)λ in aldehyde dehydrogenase 1 (ALDH1)-positive breast cancer stem cells (CSCs). MATERIALS AND

METHODS:

Breast cancer genomics datasets (TCGA, n=593; METABRIC, n=1904) were downloaded and statistically analyzed. The effects of GLO 1 and PKCλ on trypan blue staining and tumor-sphere formation by ALDH1high cells derived from triple negative breast cancer (TNBC) and basal-like breast cancer were examined.

RESULTS:

GLO 1high, PKCλhigh, and ALDH1A3high tumors were enriched in stage I/II/III/IV samples, associated with the HER2 and TNBC subtypes according to receptor status, and associated with the HER2-enriched and basal-like subtypes according to PAM50. Inhibition of either GLO 1 (TLSC702) or PKCλ (ANF) suppressed tumor-sphere formation and enhanced death in ALDH1high cells. TLSC702 also effectively inhibited tumor-sphere formation and induced death in PKCλ knockout ALDH1high cells.

CONCLUSION:

GLO 1 and PKCλ are important for the survival of ALDH1-positive breast CSCs, and may represent potential therapeutic targets for the treatment of ALDH1-positive breast CSCs.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Neoplásicas / Proteína Quinasa C / Neoplasias de la Mama / Familia de Aldehído Deshidrogenasa 1 / Isoenzimas / Lactoilglutatión Liasa Tipo de estudio: Etiology_studies Límite: Female / Humans Idioma: En Revista: Anticancer Res Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Madre Neoplásicas / Proteína Quinasa C / Neoplasias de la Mama / Familia de Aldehído Deshidrogenasa 1 / Isoenzimas / Lactoilglutatión Liasa Tipo de estudio: Etiology_studies Límite: Female / Humans Idioma: En Revista: Anticancer Res Año: 2021 Tipo del documento: Article País de afiliación: Japón