نتایج جستجو برای: cancer cell lines

تعداد نتایج: 2441499  

Ovarian cancer is the most lethal gynecological cancer in which cisplatin-based treatment plays fundamental role as the first line chemotherapy option. However, development of platinum-resistance is a critical and poorly understood problem in ovarian cancer treatment. Although in vitro generation of platinum-resistant ovarian cancer cell lines is a long established approach to uncover the molec...

Journal: :iranian journal of pharmaceutical research 0
karim ebrahim department of toxicology, school of pharmacy, shahid beheshti university of medical sciences hossein vatanpour department of toxicology, school of pharmacy, shahid beheshti university of medical sciences abbas zare razi vaccine and serum research institute farashad h.shirazi pharmaceutical sciences research center, shahid beheshti university of medical sciences maryam nakhjavani department of toxicology, school of pharmacy, shahid beheshti university of medical sciences

abstract cancer is the leading cause of death worldwide. current anticancer drugs involve various toxic side effects; efforts are ongoing to develop new anticancer agents especially from the screening of natural compounds. present study investigated cytotoxic effects and mode of cell death induced by the caspian cobra venom in some human cancer cell lines. cytotoxic effects of snake venom toxin...

Journal: :modares journal of medical sciences: pathobiology 2014
seyed hamid aghaee-bakhtiari ehsan arefian masoud soleimani siamak mirab samiee farshid noorbakhsh

objective: prostate cancer is the fifth most common cancer. in 2012, it was the second leading cause of cancer death for men worldwide. the pi3k/akt pathway plays an essential role in pathogenesis of prostate cancer; the key role of this pathway in cancer progression makes it an attractive target for prostate cancer therapy. micrornas (mirnas) that regulate gene expression have a special abilit...

Journal: :journal of reports in pharmaceutical sciences 0
hadi  adibi department of medicinal chemistry, faculty of pharmacy, kermanshah university of medical sciences, kermanshah 67145-1673, iran leila hosseizadeh maryam mahdian alireza foroumadi mohammad ali zolfigol shadpour mallakpour

a series of fluoroquinolone derivatives holding triazolidindione moieties have been synthesized and proved to be cytotoxic agents in vitro particularly against cancer cell lines (sknmc, mcf7, a2780-cp, sw48, a549, kb, ht-29, hepg 2 ). the cytotoxic activity was assessed using mtt colorimetric assay. our compounds had less cytotoxicity than doxorubicin in all studied cell lines.

Marine Streptomyces are prolific producers of majority of bioactive secondary metabolites which are used in pharmaceutical industry as effective drugs against life threatening diseases. The cytotoxic activity of the pure compound 1, 2- benzene dicarboxylic acid, mono 2- ethylhexyl ester (DMEHE) from marine derived actinomycete Streptomyces sp. VITSJK8 was investigated against mouse embryonic fi...

ژورنال: طب جنوب 2021
Ebrahimi , Seyed Omar, Reiisi , Somayeh,

Background: ncRNAs have been identified as oncogenic drivers and tumor suppressors in any type of cancer. Although many classes of ncRNAs have been reported, most studies have been performed on microRNAs (miRNAs). miRNAs can regulate several target genes and affect important processes such as homeostasis, angiogenesis, cell proliferation, differentiation, and apoptosis. Located in the p75NTR ge...

Journal: :international journal of molecular and cellular medicine 0
kannabiran krishnan school of biosciences and technology, vit university, tamilnadu, india. abirami mani school of biosciences and technology, vit university, tamilnadu, india. subashini jasmine school of biosciences and technology, vit university, tamilnadu, india.

marine streptomyces are prolific producers of majority of bioactive secondary metabolites which are used in pharmaceutical industry as effective drugs against life threatening diseases. the cytotoxic activity of the pure compound 1, 2- benzene dicarboxylic acid, mono 2- ethylhexyl ester (dmehe) from marine derived actinomycete streptomyces sp. vitsjk8 was investigated against mouse embryonic fi...

A Ahi A Emami M Mahmoudi SH Zamani Taghizadeh Rabe

Background & Aims: In most cases, drugs used for the treatment of cancer are not effective or have unpleasant side-effects. This has forced scientists to find more effective drugs with less toxicity. Artemisia is an important medicinal plant in the world and anti-tumoral activity of some Artemisia species has been reported. This study was designed for evaluation of anti-tumoral effect of methan...

Two set of 2-aryl-5,6-dihydropyrrolo[2,1-a] isoquinolines were designed and synthesized to evaluate their biological activities as topoisomerase inhibitors. Cytotoxic activity of the synthesized compounds 4a-e and 7a-d was assessed against several human cancer cell lines, including MCF-7 (breast cancer cell), HepG2 (liver hepatocellular cells), A549 (adenocarcinomic human alveolar basal epithel...

Gholamhossin Hassanshahi MalekHosein Asadi Mohammad Reza Mirzaei, Seyed Javad Mowla, Zahra Ahmadi,

Objective(s): The OCT4B1, as one of OCT4 variants, is expressed in cancer cell lines and tissues more than other variants and plays an important role in apoptosis and stress (heat shock protein) pathways. The present study was designed to determine the effects of OCT4B1 silencing on expressional profile of HSP40 gene family expression in three different human tumor cell lines. Materials and Met...

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