Expression of ADAM۱۰ and CD۵۸ in Acute and Chronic Lymphocytic Leukemia: Influence of Disease Stage and Chemotherapy

سال انتشار: 1404
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 197

فایل این مقاله در 10 صفحه با فرمت PDF قابل دریافت می باشد

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این مقاله:

شناسه ملی سند علمی:

JR_IJP-20-3_009

تاریخ نمایه سازی: 28 تیر 1404

چکیده مقاله:

Background & Objective: CD۵۸ and ADAM۱۰ have been implicated in leukemia progression and chemoresistance; however, their specific roles in acute lymphoblastic leukemia (ALL) and chronic lymphocytic leukemia (CLL), particularly under chemotherapeutic pressure, remain insufficiently characterized. This study aimed to assess the expression of CD۵۸, an immune adhesion molecule, and ADAM۱۰, a metalloproteinase, in ALL and CLL patients undergoing chemotherapy, and to explore their potential involvement in immune evasion, niche-mediated survival, and chemoresistance mechanisms.Methods: Peripheral blood mononuclear cells (PBMCs) were isolated from ۵۰ patients with ALL, ۵۰ with CLL, and ۳۰ healthy controls. Expression levels of CD۵۸ and ADAM۱۰ were analyzed by quantitative reverse transcription PCR (qRT-PCR) and flow cytometry. Chemotherapy regimens included vincristine (VCR), methotrexate (MTX), and doxorubicin (DOXO).Results: ADAM۱۰ mRNA expression was significantly upregulated in ALL patients treated with VCR+MTX (p<۰.۰۰۰۱) and DOXO (p=۰.۰۰۱), with corresponding protein overexpression observed in both ALL (p<۰.۰۰۰۱) and untreated CLL patients (p<۰.۰۰۰۱). A significant difference in ADAM۱۰ levels was noted between ALL and CLL cohorts (p=۰.۰۰۱). CD۵۸ mRNA and protein expression were markedly increased in ALL patients receiving VCR+MTX (p<۰.۰۰۰۱), whereas untreated CLL patients exhibited no significant alterations.Conclusion: CD۵۸ and ADAM۱۰ are differentially regulated in ALL under chemotherapy, supporting their roles in immune evasion and microenvironmental survival. The constitutive overexpression of ADAM۱۰ in CLL suggests its involvement in chronic leukemic pathogenesis. These findings highlight CD۵۸ and ADAM۱۰ as potential therapeutic targets for overcoming chemoresistance in lymphoid malignancies.

نویسندگان

ameer Kadhim

Department of Pathological Analyses, Faculty of Science, University of Kufa, Kufa, Najaf Governorate, Iraq

Muslim Mohsin

Department of Pathological Analyses, Faculty of Science, University of Kufa, Kufa, Najaf Governorate, Iraq

مراجع و منابع این مقاله:

لیست زیر مراجع و منابع استفاده شده در این مقاله را نمایش می دهد. این مراجع به صورت کاملا ماشینی و بر اساس هوش مصنوعی استخراج شده اند و لذا ممکن است دارای اشکالاتی باشند که به مرور زمان دقت استخراج این محتوا افزایش می یابد. مراجعی که مقالات مربوط به آنها در سیویلیکا نمایه شده و پیدا شده اند، به خود مقاله لینک شده اند :