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Lipocalin 2 inhibits actin glutathionylation to promote invasion and migration.
Choudhary, Bhagya Shree; Chaudhary, Nazia; Shah, Manya; Dwivedi, Nehanjali; P K, Smitha; Das, Manjula; Dalal, Sorab Nariman.
Affiliation
  • Choudhary BS; Cell and Tumor Biology, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.
  • Chaudhary N; Homi Bhabha National Institute, Mumbai, India.
  • Shah M; Cell and Tumor Biology, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.
  • Dwivedi N; Homi Bhabha National Institute, Mumbai, India.
  • P K S; Cell and Tumor Biology, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.
  • Das M; Molecular Immunology, Mazumdar Shaw Medical Foundation, Bommasandra, Bangalore, India.
  • Dalal SN; Product Research Group, Mazumdar Shaw Medical Foundation, Bommasandra, Bangalore, India.
FEBS Lett ; 597(8): 1086-1097, 2023 04.
Article in En | MEDLINE | ID: mdl-36650979
ABSTRACT
Invasive and metastatic tumor cells show an increase in migration and invasion, making the processes contributing to these phenotypes potential therapeutic targets. Lipocalin 2 (LCN2; also known as neutrophil gelatinase-associated lipocalin) is a putative therapeutic target in multiple tumor types and promotes invasion and migration, although the mechanisms underlying these phenotypes are unclear. The data in this report demonstrate that LCN2 promotes actin polymerization, invasion, and migration by inhibiting actin glutathionylation. LCN2 inhibits actin glutathionylation by decreasing the levels of reactive oxygen species (ROS) and by reducing intracellular iron levels. Inhibiting LCN2 function leads to increased actin glutathionylation, decreased migration, and decreased invasion. These results suggest that LCN2 is a potential therapeutic target in invasive tumors.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Actins / Neoplasms Limits: Humans Language: En Journal: FEBS Lett Year: 2023 Document type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Actins / Neoplasms Limits: Humans Language: En Journal: FEBS Lett Year: 2023 Document type: Article Affiliation country: India