نتایج جستجو برای: hela kb mda mb 468

تعداد نتایج: 84493  

Abasalt Hosseinzadeh Colagar , Alireza Rafiei, Omolbanin Amjadi , Reza Valadan,

Background: Understanding of cellular and molecular mechanisms involved in cell/tumor growth and progression has led to molecular-targeted therapy. HER1 and HER2 are two main oncogenic components of HER-receptor family considered as targets for cancer research and therapy. Reliable results of HER- related research and targeted therapies dependent upon cell line with known HER expression status....

Journal: :Molecular cancer therapeutics 2012
Muralidharan Anbalagan Alaa Ali Ryan K Jones Carolyn G Marsden Mei Sheng Latonya Carrier Yahao Bu David Hangauer Brian G Rowan

Src kinase is elevated in breast tumors that are ER/PR negative and do not overexpress HER2, but clinical trials with Src inhibitors have shown little activity. The present study evaluated preclinical efficacy of a novel peptidomimetic compound, KX-01 (KX2-391), that exhibits dual action as an Src and pretubulin inhibitor. KX-01 was evaluated as a single-agent and in combination with paclitaxel...

Journal: :Cancer research 1998
S Hiraguri T Godfrey H Nakamura J Graff C Collins L Shayesteh N Doggett K Johnson M Wheelock J Herman S Baylin D Pinkel J Gray

Loss of E-cadherin (CDH1) function is thought to contribute to progression in breast cancer and other solid tumors by increasing proliferation, invasion, and/or metastasis. In some cases, the restoration of CDH1 function may be an important therapeutic option. This possibility will depend on the mechanism by which CDH1 is inactivated. Here we present analyses of CDH1 expression, genetic mutatio...

Journal: :Tetrahedron letters 2014
Somayeh Motavallizadeh Asal Fallah-Tafti Saeedeh Maleki Amir Nasrolahi Shirazi Mahboobeh Pordeli Maliheh Safavi Sussan Kabudanian Ardestani Shaaban Asd Rakesh Tiwari Donghoon Oh Abbas Shafiee Alireza Foroumadi Keykavous Parang Tahmineh Akbarzadeh

Several novel N-(9-oxo-9H-xanthen-4-yl)benzenesulfonamides derivatives were prepared as potential antiproliferative agents. The in vitro antiproliferative activity of the synthesized compounds was investigated against a panel of tumor cell lines including breast cancer cell lines (MDA-MB-231, T-47D) and neuroblastoma cell line (SK-N-MC) using MTT colorimetric assay. Etoposide, a well-known anti...

2015
Xiaolong Wang Wenwen Qi Yaming Li Ning Zhang Lun Dong Mingjuan Sun Jinjing Cun Yan Zhang Shangge Lv Qifeng Yang Vladimir Trajkovic

Huaier extract is attracting increased attention due to its biological activities, including antitumor, anti-parasite and immunomodulatory effects. Here, we investigated the role of autophagy in Huaier-induced cytotoxicity in MDA-MB-231, MDA-MB-468 and MCF7 breast cancer cells. Huaier treatment inhibited cell viability in all three cell lines and induced various large membranous vacuoles in the...

2017
Zekun Chen Qiuju Wu Ye Ding Wenhui Zhou Rong Liu Haiying Chen Jia Zhou Jing Feng Ceshi Chen

Triple-negative breast cancer (TNBC) is an aggressive malignancy with poor clinical outcomes. YD277 is a novel small molecule derived from ML264, a KLF5 inhibitor that elicits cytotoxic effects in colon cancer cell lines. Our previous studies suggest that Krüpple-like factor 5 (KLF5) is a promising therapeutic target for TNBC. In this study, we demonstrated that YD277 significantly induced G1 c...

2017
Shuping Yin Vino T Cheryan Liping Xu Arun K Rishi Kaladhar B Reddy

Women with triple negative breast cancer (TNBC) have poor prognosis compared to other breast cancer subtypes. There were several reports indicating racial disparity in breast cancer outcomes between African American (AA) and European American (EA) women. For example, the mortality rates of AA breast cancer patients were three times higher than of EA patients, even though, the incidence is lower...

آزموده, شمیلا, ایزدیار, محمد, بابایی, مریم, شکوه‌سلجوقی, امیر,

سابقه و هدف: مطالعات نشان داده­اند که برخی لیگاندها نظیر مالتول با کئوردینه­شدن با فلزات، موجب القاء آپوپتوز و مهار تکثیر سلول­های سرطانی می­شود. هدف از این مطالعه، سنتز کمپلکس­های جدیدی از نیکل و ارزیابی اثرات آپوپتیک و ضدتکثیری این ترکیبات می­باشد. مواد و روش­ها: در این مطالعه، کمپلکس­هایی از نیکل و لیگاندهای مالتول، دیفریپرون و 3-هیدروکسی­فلاون سنتز­گردید. سایتوتوکسیسیته این کمپلکس­ها به منظ...

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