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Genetically Targeted Fractionated Chemotherapy 被引量:1

Genetically Targeted Fractionated Chemotherapy
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摘要 Complex and late stage cancer patients are in need of novel methods of selecting and administering chemotherapy particularly for those patients who are refractory to current treatment methods. The use of biomarkers to enhance decision making with regard to the molecular profile of a person’s cancer is becoming more important in the practice of oncology. The standard for the last several decades is to elect chemotherapeutic agents based on staging and histological identification of the primary cancer site alone versus utilizing the genetic and molecular profile information along with histological primary cancer site and staging to select chemotherapy regimens. Cancers are caused by mutations that occur within cells and therefore selecting treatment based on mutations and not primary cancer site alone can provide advantages that may have gone overlooked. As time progresses, more biomarkers continue to be discovered which can lead to more targets for drugs either currently on the market or clinical trials. In addition to advancements made in the progression of cancer treatment with utilizing molecular profiles effectively, there are other therapeutic strategies that have been postulated as advanced effective ways to administer chemotherapy. These strategies provide chemotherapy to patients while fasting, giving insulin or other biological response modifiers adjunctively prior to chemotherapy for enhanced targeting, and giving chemotherapy in micro-doses to allow for increased frequency of administration and the utilization of multiple targeted chemotherapeutic agents concurrently. In this paper we will discuss these topics and explain their benefits in addition to the evidence that supports these treatments. A review on biomarkers and cancer cell metabolism is discussed as it relates to providing a framework for what constitutes a biomarker in addition to what metabolic processes are related to fasting and administering insulin with chemotherapy. The information provided in this document is designed to illuminate and provide evidence for various methodologies that are underserved in the treatment of cancer. Complex and late stage cancer patients are in need of novel methods of selecting and administering chemotherapy particularly for those patients who are refractory to current treatment methods. The use of biomarkers to enhance decision making with regard to the molecular profile of a person’s cancer is becoming more important in the practice of oncology. The standard for the last several decades is to elect chemotherapeutic agents based on staging and histological identification of the primary cancer site alone versus utilizing the genetic and molecular profile information along with histological primary cancer site and staging to select chemotherapy regimens. Cancers are caused by mutations that occur within cells and therefore selecting treatment based on mutations and not primary cancer site alone can provide advantages that may have gone overlooked. As time progresses, more biomarkers continue to be discovered which can lead to more targets for drugs either currently on the market or clinical trials. In addition to advancements made in the progression of cancer treatment with utilizing molecular profiles effectively, there are other therapeutic strategies that have been postulated as advanced effective ways to administer chemotherapy. These strategies provide chemotherapy to patients while fasting, giving insulin or other biological response modifiers adjunctively prior to chemotherapy for enhanced targeting, and giving chemotherapy in micro-doses to allow for increased frequency of administration and the utilization of multiple targeted chemotherapeutic agents concurrently. In this paper we will discuss these topics and explain their benefits in addition to the evidence that supports these treatments. A review on biomarkers and cancer cell metabolism is discussed as it relates to providing a framework for what constitutes a biomarker in addition to what metabolic processes are related to fasting and administering insulin with chemotherapy. The information provided in this document is designed to illuminate and provide evidence for various methodologies that are underserved in the treatment of cancer.
机构地区 Envita
出处 《Journal of Cancer Therapy》 2015年第2期182-198,共17页 癌症治疗(英文)
关键词 Biomarkers MOLECULAR PROFILE Cancer CHEMOTHERAPY GLYCOLYSIS INSULIN Biomarkers Molecular Profile Cancer Chemotherapy Glycolysis Insulin
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  • 1[10]Nakano A,Watanabe N,Nishizaki Y,Takashimizu S,Matsuzaki S.Immunohistochemical studies on the expression of P-glycoprotein and p53 in relation to histological differentiation and cell proliferation in hepatocellular carcinoma.Hepatol Res 2003; 25:158-165
  • 2[11]Goldstein LJ,Galski H,Fojo A,Willingham M,Lai SL,Gazdar A,Pirker R,Green A,Crist W,Brodeur GM.Expression of a multidrug resistance gene in human cancers.J Natl Cancer Inst 1989; 81:116-124
  • 3[12]Chin KV,Ueda K,Pastan I,Gottesman MM.Modulation of activity of the promoter of the human MDR1 gene by Ras and p53.Science 1992; 255:459-462
  • 4[13]Goldsmith ME,Gudas JM,Schneider E,Cowan KH.Wild type p53 stimulates expression from the human multidrug resistance promoter in a p53-negative cell line.J Biol Chem 1995;270:1894-1898
  • 5[14]Baldini N,Scotlandi K,Barbanti-Brodano G,Manara MC,Maurici D,Bacci G,Bertoni F,Picci P,Sottili S,Campanacci M.Expression of P-glycoprotein in high-grade osteosarcomas in relation to clinical outcome.N Engl J Med 1995; 333:1380-1385
  • 6[15]Chan HS,Haddad G,Thorner PS,DeBoer G,Lin YP,Ondrusek N,Yeger H,Ling V.P-glycoprotein expression as a predictor of the outcome of therapy for neuroblastoma.N Engl J Med 1991; 325:1608-1614
  • 7[16]Cole SP,Chanda ER,Dicke FP,Gerlach JH,Mirski SE.NonP-glycoprotein-mediated multidrug resistance in a small cell lung cancer cell line:evidence for decreased susceptibility to drug-induced DNA damage and reduced levels of topoisomerase Ⅱ.Cancer Res 1991; 51:3345-3352
  • 8[17]Minemura M,Tanimura H,Tabor E.Overexpression of multidrug resistance genes MDR1 and cMOAT in human hepatocellular carcinoma and hepatoblastoma cell lines.Int J Oncol 1999; 15:559-563
  • 9[18]Nishio M,Koshikawa T,Kuroishi T,Suyama M,Uchida K,Takagi Y,Washimi O,Sugiura T,Ariyoshi Y,Takahashi T,Ueda R,Takahashi T.Prognostic significance of abnormal p53accumulation in primary,resected non-small-cell lung cancers.J Clin Oncol 1996; 14:497-502
  • 10[19]Muller M,Strand S,Hug H,Heinemann EM,Walczak H,Hofmann WJ,Stremmel W,Krammer PH,Galle PR.Drug-induced apoptosis in hepatoma cells is mediated by the CD95 (APO-1/Fas) receptor/ligand system and involves activation of wildtype p53.J Clin Invest 1997; 99:403-413

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