نتایج جستجو برای: du145
تعداد نتایج: 1417 فیلتر نتایج به سال:
BACKGROUND Thapsigargin (TG) is a potent inhibitor of sarcoplasmic/endoplasmic reticulum Ca2+ ATPases (SERCAs). TG-based prodrugs are being developed for the treatment of prostate cancer (PC). To develop optimal TG-based therapeutics it is important to understand the mechanisms of resistance to TG that may potentially occur in cancer cells. METHODS DU145/TG and PC3/TG cells were derived from ...
زمینه و هدف: سرطان پروستات شایع ترین سرطان در جامعه مردان است. عوامل بسیار زیادی منجر به بروز این بیماری می شود. در عین حال فاکتورهای متعددی به منظور پیشگیری و یا درمان این بیماری شناسایی شده اند. آنتی اکسیدان ها و مخصوصاً ترکیبات پلی فنلی مانند اسید گالیک دارای ظرفیت بالقوه ای از این ویژگی هستند. در این مطالعه با استفاده از تکنیک الکتروفورز قلیایی، اثر اسید گالیک را بر لاین سلول های سرطانی du14...
یکی از داروهای رایج در درمان سرطان پروستات داکسوروبیسین است. داکسوروبیسین علاوه بر تاثیر بر سلول ها و بافت های سرطانی دارای عوارض جانبی بر بافت های سالم نیز می باشد. به-منظور افزایش تاثیر این دارو بر سلول های سرطانی و کاهش اثرات سمیت سلولی حاصل از آن بر سلول ها و بافت های سالم، از روش های ترکیبی همانند به کارگیری داکسوروبیسین در حضور نانوذرات (به عنوان عامل حساس به نور) و پرتو استفاده می-شود. د...
Background . Melittin is a major constituent of honeybee venom and comprises water-soluble surfactant peptide with cytolytic effects potentially applicable in anticancer therapy. We evaluated the impact melittin from Bashkir ( Apis mellifera L.) on cell viability various prostate cancer lineages. Materials methods. MTT assays index estimation were used to evaluate effect proliferation various-g...
Genotoxic treatments elicit DNA damage response (DDR) not only in cells that are directly exposed but also in cells that are not in the field of treatment (bystander cells), a phenomenon that is commonly referred to as the bystander effect (BE). However, mechanisms underlying the BE remain elusive. We report here that etoposide and ultraviolet (UV) exposure stimulate the production of microvesi...
Abstract Background About 90% of cancer-related deaths are due to metastasis cancer cells, and angiogenesis is a critical step in this process. sFLT01 novel fusion protein dual-targeting agent that neutralizes both VEGF PlGF proangiogenic activities. GRP78 dual effect tumor growth could be activated under stimulation. The current study was designed investigate the inhibitory impact on VEGF/GRP7...
BACKGROUND Although paclitaxel is used for hormone-resistant prostate cancer, relapse definitely occurs later. Details of the molecular mechanism responsible for paclitaxel- resistance remain unclear. METHODS We established paclitaxel-resistant cells, DU145-TxR and PC-3-TxR from parent DU145 and PC-3. To characterize these cells, we examined cross-resistance to other anticancer drugs. Express...
The mechanisms underlying prostate cancer progression are poorly understood. Proteins responsive to androgens may be involved in the development and progression of prostate cancer and the ultimate failure of androgen-ablation therapy. Therapy with somatostatin (sms) analogues could be a possible therapeutic alternative to chemotherapy in hormone refractory prostate cancer patients. We used two ...
The prostate tumor-inducing gene 1 (PTI-1) was originally identified by differential ribonucleic acid (RNA) display in human prostate carcinoma. PTI-1 is expressed in human prostate carcinoma but not in benign prostate hypertrophy or normal prostate tissue. PTI-1 may be a member of oncogenes that could affect protein translation and contribute to carcinoma development in human prostate. To inve...
BACKGROUND Sodium butyrate, a histone deacetylase inhibitor, has emerged as a promising anticancer drug for multiple cancers. Recent studies have indicated that sodium butyrate could inhibit the progression of prostate cancer; however, the exact mechanism is still unclear. The aim of this study was to investigate the mechanism of sodium butyrate action in prostate cancer DU145 cells. METHODS ...
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