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485 Newest Publications in molecular carcinogenesis
rss03-03-2011 | Fu, Huijing; Zhang, Jingjie; Pan, Jing; Zhang, Qi; Lu, Yan; Wen, Weidong; Lubet, Ronald A.; Szabo, Eva; Chen, Ruth; ..., Molecular Carcinogenesis, 2011
Abstract Budesonide, a synthetic glucocorticoid used for treating asthma, and pioglitazone, a synthetic peroxisome proliferator‐activated receptors γ ligand used for the treatment of diabetes, were evaluated for their combinational chemopreventive efficacy on mouse lung cancer using female ...
03-03-2011 | Monroy, Claudia M.; Cortes, Andrea C.; Lopez, Mirtha; Rourke, Elizabeth; Etzel, Carol J.; Younes, Anas; Strom, Sara ..., Molecular Carcinogenesis, 2011
Abstract DNA repair variants may play a potentially important role in an individual's susceptibility to developing cancer. Numerous studies have reported the association between genetic single nucleotide polymorphisms (SNPs) in DNA repair genes and different types of hematologic cancers. ...
03-03-2011 | Thomsen, Rune; Christensen, Dennis B.; Rosborg, Sanne; Linnet, Toke E.; Blechingberg, Jenny; Nielsen, Anders L., Molecular Carcinogenesis, 2011
Abstract The three mammalian HP1 proteins, HP1α/CBX5, HP1β/CBX1, and HPγ/CBX3, are involved in chromatin packing and gene regulation. The HP1α protein is down‐regulated in invasive compared to non‐invasive breast cancer cells and HP1α is a suppressor of cell migration and invasion. In this ...
01-03-2011 | Elena Grau; Francisco Martinez; Carmen Orellana; Adela Canete; Yania Yañez; Silvestre Oltra; Rosa Noguera; Miguel He ..., Molecular Carcinogenesis, 2011
Abstract Neuroblastoma (NB) is an embryonal tumour of neuroectodermal cells, and its prognosis is based on patient age at diagnosis, tumour stage and MYCN amplification, but it can also be classified according to their degree of methylation. Considering that epigenetic aberrations could ...
01-03-2011 | DiNatale, Brett C.; Schroeder, Jennifer C.; Perdew, Gary H., Molecular Carcinogenesis, 2011
Abstract There is increasing evidence that the aryl hydrocarbon receptor (AHR) plays a role in tumor progression through numerous mechanisms. We have previously shown that, in certain cancer cell lines that are typically nonresponsive to cytokine‐mediated IL6 induction, activation of the ...
01-03-2011 | Choudhary, Shambhunath; Wang, Kwo‐Kwang Abraham; Wang, Hwa‐Chain Robert, Molecular Carcinogenesis, 2011
Abstract More than 35% of human urinary bladder cancers involve oncogenic H‐Ras activation. The goal of this study was to investigate the role of the ERK pathway in mediating apoptotic signals induced by oncogenic H‐Ras, FK228 treatment, and exogenous H2O2 treatment to increase Nox‐1 ...
01-03-2011 | Zhou, Yong; Li, Ni; Zhuang, Wen; Wu, Xiaoting, Molecular Carcinogenesis, 2011
Abstract The association between vascular endothelial growth factor (VEGF) gene polymorphisms and gastric cancer risk is still controversial and ambiguous. The objective of this study was to investigate the association between VEGF gene polymorphisms and gastric cancer risk in Chinese Han ...
01-03-2011 | Yang, Zhi‐Hui; Dai, Qiong; Zhong, Li; Zhang, Xu; Guo, Qing‐Xi; Li, Shi‐Ning, Molecular Carcinogenesis, 2011
Abstract Previous studies demonstrated that the polymorphism of interleukin‐1 (IL‐1) produce alterations of the protein expression and may contribute to oncogenetic processes. The aim of this study was to investigate the relationship between IL‐1A gene polymorphisms and NPC susceptibility ...
01-03-2011 | McCallum, Gordon P.; Siu, Michelle; Ondovcik, Stephanie L.; Sweeting, J. Nicole; Wells, Peter G., Molecular Carcinogenesis, 2011
Abstract Genotoxicity tests indicate methanol (MeOH) is not mutagenic, but a rodent study has suggested carcinogenic potential, which could result from free radical‐initiated oxidative DNA damage. To investigate this possibility we treated male CD‐1 mice, New Zealand white rabbits, and ...
01-03-2011 | Wu, Yinyin; Jin, Mingjuan; Liu, Bing; Liang, Xia; Yu, Yunxian; Li, Qilong; Ma, Xinyuan; Yao, Kaiyan; Chen, Kun, Molecular Carcinogenesis, 2011
Abstract The xeroderma pigmentosum complementation group C (XPC) is responsible for removal of bulky helix‐distorting DNA lesions. Several polymorphisms of XPC gene may modulate the colorectal cancer (CRC) susceptibility. We assessed the association of XPC Lys939Gln (A/C), Ala499Val (C/T), ...
