Cancer combination therapies by silencing of CTLA-4, PDL1 and TIM3 in osteosarcoma

Cancer combination therapies by silencing of CTLA-4, PDL1, and TIM3 in osteosarcoma


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نویسندگان: امین دائی سرخابی , آیلا سرکش , علی فتوحی ملکی , حسین سعیدی , لیلی عاقبتی

کلمات کلیدی: CTLA-4, immune checkpoint, immunotherapy, osteosarcoma, PD-L1, TIM3

نشریه: 16801 , -9 , 74 , 2022

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نویسنده ثبت کننده مقاله لیلی عاقبتی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ایمونولوژی
کد مقاله 78939
عنوان فارسی مقاله Cancer combination therapies by silencing of CTLA-4, PDL1 and TIM3 in osteosarcoma
عنوان لاتین مقاله Cancer combination therapies by silencing of CTLA-4, PDL1, and TIM3 in osteosarcoma
ناشر 5
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Osteosarcoma (OS) is the most common orthopedic neoplasm, with a high metastasis rate and a dismal prognosis despite surgery and chemotherapy. Immunotherapies have offered cancer patients a ray of optimism, but their impact on OS has been disappointing. The objective of this study is to assess the effect of mono, dual, and triple combinations of CTLA-4, PD-L1, and TIM3 blockade on OS cell viability, apoptosis, and migration. The MG-63 and U-2 OS cell lines were transfected with mono, dual, and triple combinations of siRNAs specific for CTLA-4, PD-L1, and TIM3. After evaluation for transfection efficacy by qRT-PCR, MTT assay and flow cytometry were applied to assess cell viability and apoptosis rate in siRNA-transfected cells, respectively. Ultimately, the migration of transfected cells was measured by wound-healing assay. First, the qRT-PCR analysis revealed that in siRNA-transfected OS cells, CTLA-4, PD-L1, and TIM3 were downregulated. The MTT assay and flow cytometry results confirmed that silencing of these immune checkpoints in dual or triple combinations, but not in the single-agent blockade, significantly decreases cell viability and increases apoptosis, respectively. These effects were more significant when triple silencing was performed. Finally, the wound-healing assay revealed that dual and triple silencing of immune checkpoints significantly inhibits cell migration, with triple silencing exhibiting a greater effect. Our findings suggest that triple blockade of CTLA-4, PD-L1, and TIM3 is an effective strategy for inhibiting tumor cell progression and migration in OS, whichrequires large-scale clinical investigations to be translated into broad therapeutic applicability for OS patients.

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نویسنده نفر چندم مقاله
امین دائی سرخابیاول
آیلا سرکشدوم
علی فتوحی ملکیسوم
حسین سعیدیچهارم
لیلی عاقبتیپنجم

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Cancer combination therapies by in osteosarcoma.pdf1401/03/281987110دانلود