Results 71 to 80 of about 112,964 (206)

Cisplatin resistance and opportunities for precision medicine

open access: yesPharmacological Research, 2016
Cisplatin is one of the most commonly used chemotherapy drugs, treating a wide range of cancer types. Unfortunately, many cancers initially respond to platinum treatment but when the tumor returns, drug resistance frequently occurs. Resistance to cisplatin is attributed to three molecular mechanisms: increased DNA repair, altered cellular accumulation,
openaire   +2 more sources

New precious metal compounds in cancer therapy

open access: yes, 2008
Includes abstract.Includes bibliographical references (leaves 139-160).Cisplatin is one of the most effective cancer medications currently available. However, it is seriously limited by patient toxicity and drug resistance.
Peters, Dean Douglas
core  

Design, Synthesis, and Biological Activity of a Novel Non-Cisplatin-type Platinum−Acridine Pharmacophore

open access: yes, 2016
Platinum−acridine conjugates were prepared from [PtCl2(ethane-1,2-diamine)] and the novel acridinylthioureas MeHNC(S)NMeAcr (6) and MeHNC(S)NMe(CH2CH2)NHAcr (15) by replacing one chloro leaving group in the cisplatin analogue with thiourea sulfur.
Elizabeth T. Martins (3012990)   +6 more
core   +1 more source

CDKN3 promotes tumor progression and confers cisplatin resistance via RAD51 in esophageal cancer

open access: yes, 2019
Jiansong Wang,1 Wencheng Che,2 Weimin Wang,1 Gongzhang Su,3 Tianchang Zhen,3 Zhongmin Jiang31Graduate Department, Weifang Medical University, Weifang, Shandong 261031, People’s Republic of China; 2Department of Thoracic Surgery, Zibo Central ...
Jiang Z   +5 more
core  

Molecular mechanisms of cisplatin resistance in lung cancer

open access: yes, 2013
Cisplatin is one of the most potent anticancer agents, displaying significant clinical activity against a variety of solid tumours. To date, cisplatin-based combination treatment remains the most effective systemic chemotherapy for non-small cell lung ...
O'Byrne, K., Barr, M.P.
core  

Role of Autophagy in Cisplatin Resistance of Retinoblastoma Y79 Cells and Its Mechanism

open access: yesZhongliu Fangzhi Yanjiu, 2018
Objective To investigate the role of autophagy in cisplatin resistance of retinoblastoma Y79 cells and its mechanism. Methods The IC50 of cells was detected by CCK-8 assay. Y79 cells were randomly divided into control group, Cisplatin group and cisplatin
LIU Ying, SU Jie, WANG Linhong
doaj   +1 more source

一系列對cisplatin具不等程度抗藥性之移型上皮癌細胞株的抗藥性機轉研究

open access: yes, 2009
We explored the mechanisms of cisplatin resistance in a series of bladder transitional carcinoma cells that are either sensitive or progressively resistant to cisplatin.
侯自銓;陳淳;黃昭淵;官靜儀;呂秀慧;謝長堯;蒲永孝   +1 more
core  

MECHANISM OF APOPTOSIS INHIBITION TO SQUAMOUS CELL CARCINOMA OF ORAL CANCER IN CISPLATIN TREATMENT

open access: yesFolia Medica Indonesiana, 2017
This study was to approve the increased secretion of Hsp 70, DNA damage, and inhibitor apoptosis protein in cisplatin therapy which influence apoptosis of oral cancer cell and to know mechanism of molecular pathology.
R Marjono Dwi Wibowo   +2 more
doaj   +1 more source

miR-133b reverses cisplatin resistance by targeting GSTP1 in cisplatin-resistant lung cancer cells

open access: yesInternational Journal of Molecular Medicine, 2018
MicroRNAs play a critical role in chemoresistance and are implicated in various biological and pathological processes of cells. The objective of the present study was to explore the role of miR‑133b and its mechanism in the regulation of cisplatin resistance and tumor progression in cisplatin‑resistant non‑small cell lung cancer (NSCLC) cells.
Lin, Chen   +4 more
openaire   +3 more sources

The Role of Epigenetics in Resistance to Cisplatin Chemotherapy in Lung Cancer

open access: yes, 2011
Non-small cell lung cancer (NSCLC) is the most common cause of cancer related death in the world. Cisplatin and carboplatin are the most commonly used cytotoxic chemotherapeutic agents to treat the disease.
O\u27BYRNE, KEN   +8 more
core   +1 more source

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