نتایج جستجو برای: chemotherapeutics

تعداد نتایج: 2329  

2017
Manabu KOIKE Yasutomo YUTOKU Aki KOIKE

Understanding the molecular mechanisms of DNA double-strand break (DSB) repair machinery, specifically non-homologous DNA-end joining (NHEJ), is crucial for developing next-generation radiotherapies and common chemotherapeutics for human and animal cancers. The localization, protein-protein interactions and post-translational modifications of core NHEJ factors, might play vital roles for regula...

2016
Máire-Caitlín Casey Karl J Sweeney James Andrew Lawrence Brown Michael J Kerin

Breast cancer is the most frequently diagnosed malignancy amongst females worldwide. In recent years the management of this disease has transformed considerably, including the administration of chemotherapy in the neoadjuvant setting. Aside from increasing rates of breast conserving surgery and enabling surgery via tumour burden reduction, use of chemotherapy in the neoadjuvant setting allows m...

2014
Sylwia Flis Agnieszka Gnyszka Krzysztof Flis

DNA methylation is an epigenetic phenomenon known to play an important role in the development and progression of human cancer. Enzyme responsible for this process is DNA methyltransferase 1 (DNMT1) that maintains an altered methylation pattern by copying it from parent to daughter DNA strands after replication. Aberrant methylation of the promoter regions of genes critical for normal cellular ...

2013
Rachel C. Botham

Relief of procaspase inhibition enhances the potency of cancer chemotherapeutics Botham RC, Fan TM, Hergenrother PJ Manipulation of the apoptotic cascade is an effective and commonly employed strategy for the eradication of cancer cells. This work utilizes the small molecule PAC-1 to target the labile zinc pool, a physiological inhibitor of apoptosis. Labile zinc inhibits the conversion of proc...

Journal: :Molecular cancer therapeutics 2007
Joshua L Fischer Elaine M Mihelc Karen E Pollok Martin L Smith

Selenium in various chemical forms has been the subject of cancer chemoprevention trials, but, more recently, selenium has been used in combination with DNA-damaging chemotherapeutics. Specifically, selenium protected tissues from dose-limiting toxicity and, in fact, allowed delivery of higher chemotherapeutic doses. At the same time, selenium did not protect cancer cells. Therefore, we seek to...

Journal: :Molecular imaging 2012
Hui-li Ma Qiao Jiang Siyuan Han Yan Wu Jin Cui Tomshine Dongliang Wang Yaling Gan Guozhang Zou Xing-Jie Liang

We present a flexible and highly reproducible method using three-dimensional (3D) multicellular tumor spheroids to quantify chemotherapeutic and nanoparticle penetration properties in vitro. We generated HeLa cell-derived spheroids using the liquid overlay method. To properly characterize HeLa spheroids, scanning electron microscopy, transmission electron microscopy, and multiphoton microscopy ...

Journal: :Molecular pharmacology 2013
Alexandra E Stacy Patric J Jansson Des R Richardson

The ATP-binding cassette, subfamily G, isoform 2 protein (ABCG2) is an important member of the ABC transporter superfamily, which has been suggested to be involved in multidrug resistance (MDR) in cancer. Its diverse range of substrates includes many common chemotherapeutics such as imatinib, doxorubicin, and mitoxantrone. Physiologically, ABCG2 is highly expressed in areas such as the blood-br...

Journal: :Oncology reports 2012
Koji Tanaka Masato Okigami Yuji Toiyama Yuki Morimoto Kohei Matsushita Mikio Kawamura Kiyoshi Hashimoto Susumu Saigusa Yoshinaga Okugawa Yasuhiro Inoue Keiichi Uchida Toshimitsu Araki Yasuhiko Mohri Akira Mizoguchi Masato Kusunoki

In vivo real-time visualization of chemotherapy response at the cellular level provides us with direct evidence of what happens on the tumor microenvironment of metastatic organs. We imaged the response of metastatic tumor cells and host stromal cells to chemotherapeutics on liver metastatic xenografts in living mice using intravital two-photon la...

2015
Benny Zhitomirsky Yehuda G. Assaraf

Multidrug resistance (MDR) is a primary hindrance to curative cancer chemotherapy. In this respect, lysosomes were suggested to play a role in intrinsic MDR by sequestering protonated hydrophobic weak base chemotherapeutics away from their intracellular target sites. Here we show that intrinsic resistance to sunitinib, a hydrophobic weak base tyrosine kinase inhibitor known to accumulate in lys...

Journal: :Cancer discovery 2013
Tito Fojo Susan Bates

Given the malleable nature of cancer cells, we should expect, and do see, the development of resistance to any new chemotherapeutic agent. Models that help us understand how this happens are a first step to better and more effective chemotherapeutics.

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