Lysophosphatidic acid promotes survival of T lymphoma cells by altering apoptosis and glucose metabolism
Autor: | Pradip Kumar Jaiswara, Pratishtha Sonker, Rajan Kumar Tiwari, Ajay Kumar, Vishal Gupta, Shiv Govind Rawat |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Cancer Research Pyruvate dehydrogenase kinase Cell Survival T cell Clinical Biochemistry Pharmaceutical Science Apoptosis Carbohydrate metabolism Lymphoma T-Cell 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Cell Line Tumor Lysophosphatidic acid medicine Humans T-cell lymphoma Pharmacology biology Biochemistry (medical) Glucose transporter Cell Biology medicine.disease Glucose 030104 developmental biology Monocarboxylate transporter 1 medicine.anatomical_structure chemistry 030220 oncology & carcinogenesis Cancer research biology.protein lipids (amino acids peptides and proteins) Lysophospholipids Reactive Oxygen Species Pyruvate kinase |
Zdroj: | Apoptosis. 25:135-150 |
ISSN: | 1573-675X 1360-8185 |
DOI: | 10.1007/s10495-019-01585-1 |
Popis: | Lysophosphatidic acid (LPA) is a bioactive lipid, which plays an indispensable role in various physiological and pathological processes. Moreover, an elevated level of LPA has been observed in malignancies of different origins and implicated in their progression via modulation of proliferation, apoptosis, invasion and metastasis. Interestingly, few recent reports suggest a pivotal role of LPA-modulated metabolism in oncogenesis of ovarian cancer. However, little is understood regarding the role of LPA in the development and progression of T cell malignancies, which are considered as one of the most challenging neoplasms for clinical management. Additionally, mechanisms underlying the LPA-dependent modulation of glucose metabolism in T cell lymphoma are also not known. Therefore, the present study was undertaken to explore the role of LPA-altered apoptosis and glucose metabolism on the survival of T lymphoma cells. Observations of this investigation suggest that LPA supports survival of T lymphoma cells via altering apoptosis and glucose metabolism through changing the level of reactive species, namely nitric oxide and reactive oxygen species along with expression of various survival and glucose metabolism regulatory molecules, including hypoxia-inducible factor 1-alpha, p53, Bcl2, and glucose transporter 3, hexokinase II, pyruvate kinase muscle isozyme 2, monocarboxylate transporter 1, pyruvate dehydrogenase kinase 1. Taken together' the results of the present investigation decipher the novel mechanisms of LPA-mediated survival of T lymphoma cells via modulation of apoptosis and glucose metabolism. |
Databáze: | OpenAIRE |
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