کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5861850 | 1133766 | 2014 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Use of in vitro human keratinocyte models to study the effect of cooling on chemotherapy drug-induced cytotoxicity
ترجمه فارسی عنوان
استفاده از مدل های کراتینوسیت انسانی در آزمایشگاه به منظور بررسی اثر خنک کننده بر روی سمیت سلولی ناشی از داروهای شیمی درمانی
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کلمات کلیدی
NHEKEGFKSFM4-hydroxycyclophosphamideFBSBPETACROS - ROSchemotherapy-induced alopecia - آلوپسی ناشی از شیمی درمانیCytoprotection - حفاظت از سیتوfetal bovine serum - سرم جنین گاوCooling - سرمایش Cytotoxicity - سمیت سلولیCIA - سیاChemotherapy - شیمیدرمانیepidermal growth factor - عامل رشد اپیدرمیbovine pituitary extract - عصاره هیپوفیز گاوKeratinocytes - کراتینوسیتkeratinocyte serum-free medium - کراتینوسیت بدون سرمnormal human epidermal keratinocytes - کراتینوسیت های اپیدرمی طبیعی انسانReactive oxygen species - گونههای فعال اکسیژن
موضوعات مرتبط
علوم زیستی و بیوفناوری
علوم محیط زیست
بهداشت، سم شناسی و جهش زایی
چکیده انگلیسی
A highly distressing side-effect of cancer chemotherapy is chemotherapy-induced alopecia (CIA). Scalp cooling remains the only treatment for CIA, yet there is no experimental evidence to support the cytoprotective capacity of cooling. We have established a series of in vitro models for the culture of human keratinocytes under conditions where they adopt a basal, highly-proliferative phenotype thus resembling the rapidly-dividing sub-population of native hair-matrix keratinocytes. Using a panel of chemotherapy drugs routinely used clinically (docetaxel, doxorubicin and the active metabolite of cyclophosphamide 4-OH-CP), we demonstrate that although these drugs are highly-cytotoxic, cooling can markedly reduce or completely inhibit drug cytotoxicity, in agreement with clinical observations. By contrast, we show that cytotoxicity caused by specific combinatorial drug treatments cannot be adequately attenuated by cooling, supporting data showing that such treatments do not always respond well to cooling clinically. Importantly, we provide evidence that the choice of temperature may be critical in determining the efficacy of cooling in rescuing cells from drug-mediated toxicity. Therefore, despite their reductive nature, these in vitro models have provided experimental evidence for the clinically-reported cytoprotective role of cooling and represent useful tools for future studies on the molecular mechanisms of cooling-mediated cytoprotection.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology in Vitro - Volume 28, Issue 8, December 2014, Pages 1366-1376
Journal: Toxicology in Vitro - Volume 28, Issue 8, December 2014, Pages 1366-1376
نویسندگان
Wafaa Al-Tameemi, Christopher Dunnill, Omar Hussain, Manon M. Komen, Corina J. van den Hurk, Andrew Collett, Nikolaos T. Georgopoulos,