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Triangle collaboration assessment of autophagy, ER stress and hypoxia in leukemogenesis: a bright perspective on the molecular recognition of B-ALL

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Taylor & Francis Group2019-07-22 更新2026-04-16 收录
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https://tandf.figshare.com/articles/Triangle_collaboration_assessment_of_autophagy_ER_stress_and_hypoxia_in_leukemogenesis_a_bright_perspective_on_the_molecular_recognition_of_B-ALL/8976677/1
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B-lineage acute lymphoblastic leukemia (B-ALL) is the most common acute leukemia in childhood and adults, which caused by many various crystalline and unclear agents. Owning to this matter, no significant progress has been made in the patients-recovery. Recently, autophagy pathway is considered as an ambiguous agent in leukemia evaluation. We aim to discover the expression levels of upstream autophagy-regulating genes in newly diagnosed B-ALL patients. In B-ALL group, <i>BECN1</i>, <i>HIF1A</i> and <i>ERN1</i> expressions were significantly down-regulated, while <i>BCL2</i> expression was up-regulated compared to the control group (<i>p</i> BECN1 compared with Hypoxia and endoplasmic reticulum (ER) stress-related genes expression in the patients (<i>p</i> ERN1 and ER stress pathway-related genes could be effective regulators of autophagy in B-ALL. More investigation is recommended to gain a deeper understanding into molecular pathophysiology of B-ALL to improve treatment and monitoring approaches in affected patients.
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2019-07-22
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