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Titlebook: DNA Repair in Cancer Therapy; Lawrence C. Panasci,Moulay A. Alaoui-Jamali Book 2004 Springer Science+Business Media New York 2004 BRCA.DNA

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发表于 2025-3-21 19:29:32 | 显示全部楼层 |阅读模式
书目名称DNA Repair in Cancer Therapy
编辑Lawrence C. Panasci,Moulay A. Alaoui-Jamali
视频video
概述Includes supplementary material:
丛书名称Cancer Drug Discovery and Development
图书封面Titlebook: DNA Repair in Cancer Therapy;  Lawrence C. Panasci,Moulay A. Alaoui-Jamali Book 2004 Springer Science+Business Media New York 2004 BRCA.DNA
描述A comprehensive review of the recent developments in DNA repair that have potential for translational and clinical applications. The authors explain in detail the various mechanisms by which cancer cells can circumvent anticancer therapy and limits its usefulness in patients. They also review the clinical impact of such novel inhibitors of DNA repair mechanisms as methylguanine-DNA-methyltransferase. Also examined are inhibitors of other DNA repair enzymes such as PARP and DNA-PK, now under development and close to clinical trials. The book captures-for both cancer researchers and practicing oncologists dealing with hallmark "relapse" or "drug resistance" phenomena on a daily basis-the many exciting new uses of DNA repair inhibitors, either alone or in combination with anticancer therapies.
出版日期Book 2004
关键词BRCA; DNA; apoptosis; cancer treatment; cell; cell death; clinical trial; prevention; radiotherapy; tumor; tum
版次1
doihttps://doi.org/10.1007/978-1-59259-735-2
isbn_softcover978-1-61737-480-7
isbn_ebook978-1-59259-735-2Series ISSN 2196-9906 Series E-ISSN 2196-9914
issn_series 2196-9906
copyrightSpringer Science+Business Media New York 2004
The information of publication is updating

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发表于 2025-3-22 00:17:03 | 显示全部楼层
Role of Nonhomologous End-Joining and Recombinational DNA Repair in Resistance to Nitrogen Mustard sported by carrier-mediated systems into cells and alkylate DNA, RNA, and proteins .. Alkylation of DNA and, more specifically, the formation of DNA interstrand crosslinks have been considered to be responsible for their cytotoxicity .. Resistance to the nitrogen mustards in murine and human tumor c
发表于 2025-3-22 00:48:26 | 显示全部楼层
Repair of DNA Interstrand Crosslinks Produced by Cancer Chemotherapeutic Drugs,uch as the nitrogen mustards .. DNA was later identified as a target for these drugs ., and the covalent modification of DNA almost certainly accounts for the antitumor activity of these drugs (1). The fact that a bifunctional covalent reaction with DNA (crosslinking) is essential for the toxicity o
发表于 2025-3-22 08:18:59 | 显示全部楼层
Chemosensitization to Platinum-Based Anticancer Drugs,ad, neck, and lung. Cisplatin shows considerable efficacy in the treatment of testicular cancers with cure rates of greater than 90% .. Despite its remarkable success in the treatment of cancer, its efficacy is limited by acquired or intrinsic resistance, and the mechanisms underlying chemoresistanc
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Regulation of DNA Repair and Apoptosis by p53 and Its Impact on Alkylating Drug Resistance of Tumoregregation. This protective mechanism is essential for maintaining genomic integrity and stability, cell viability, and prevention of mutations. The drugs used in the treatment of human malignancies are invariably genotoxic, and their effectiveness is limited by a variety of factors. The most import
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Stress-Activated Signal Transduction Pathways in DNA Damage Response, cells develop an impressive arsenal of constitutive and/or inducible DNA-damage response mechanisms, which can deregulate the cell cycle checkpoints and DNA repair and allow cells to escape from apoptotic cell death.
发表于 2025-3-22 20:40:47 | 显示全部楼层
Overcoming Resistance to Alkylating Agents by Inhibitors of ,,-Alkylguanine-DNA Alkyltransferase,or these agents and the correct repair of DNA damage provides protection from them .. Virtually every DNA repair pathway is able to interact with one or more facets of alkylation damage. Alkylated bases are repaired via base excision repair (BER), nucleotide excision repair (NER), and direct reversa
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发表于 2025-3-23 02:18:24 | 显示全部楼层
Potential Role of PARP Inhibitors in Cancer Treatment and Cell Death,c integrity (reviewed in refs. . and .). DNA damage induces a 10- to 500-fold increase in PARP-1 activity, which causes a drastic lowering of the cellular NAD. content. PARP-1 binds to DNA strand breaks and hydrolyzes NAD. to synthesize poly(ADP-ribose) chains (pADPr) on nuclear protein substrates,
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Relationship Among DNA Repair Genes, Cellular Radiosensitivity, and the Response of Tumors and Normlinically determined tolerance of the normal tissues in the radiation field .. The optimization of XRT treatment plans involves the computation of two factors for a given dose prescription: the tumor control probability (TCP) and the normal tissue complication probability (NTCP). The therapeutic out
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