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DISEASE MODEL NEW

外国特許コード F200010233
整理番号 (S2019-0209-N0)
掲載日 2020年10月29日
出願国 世界知的所有権機関(WIPO)
国際出願番号 2020JP003159
国際公開番号 WO2020158794
国際出願日 令和2年1月29日(2020.1.29)
国際公開日 令和2年8月6日(2020.8.6)
優先権データ
  • 特願2019-014778 (2019.1.30) JP
発明の名称 (英語) DISEASE MODEL NEW
発明の概要(英語) The present invention provides a method for producing a disease model, the method including a step for introducing cancer cells or fibroblasts into recellularized organs or tissue.
従来技術、競合技術の概要(英語) BACKGROUND ART
Cancer is 1 major factors of human death. Studies on methods of treatment of cancer have been actively progressed, but the 5-year survival rate remains low, for example, in the case of lung cancer, the 5-year survival rate of lung cancer patients remains at about 15 %. In recent years, development of anticancer agents targeting molecules expressed in cancer has been progressed, and as the target 1, epidermal growth factor receptor (EGFR), which is recognized to be overexpressed in various malignant tumors such as non-small cell lung cancer (NSCLC), has been focused. For example, it has been reported that administration of a EGFR inhibitor has an antitumor effect to NSCLC patients with a EGFR mutation that causes EGFR activation. However, there is also reported a problem that the number of patients having the gene mutation is small, and the secondary mutation of the gene causes cancer cells to have drug resistance, for example, Non-Patent Document 1). Therefore, in order to provide drugs and combinations of drugs for treating diseases such as cancer suitable for individual patients, it is believed that understanding of biological mechanisms of diseases including diversity and mechanism of acquisition of resistance is indispensable (, for example, Non-Patent Document 2).
Fibrosis is a disease in which abnormal accumulation of fibrotic tissue due to tissue damage, autoimmune reaction, and the like is recognized, and fibrosis in various organs and tissues such as lung, liver, pancreas, kidney, heart, bone marrow, and skin is known in humans. Fibrosis whose cause can be identified is often cured by removal of the cause or administration of anti-inflammatory agents such as steroids. On the other hand, steroids and immunosuppressants are generally used for the treatment of pulmonary fibrosis and interstitial pneumonia accompanied by fibrosis, but there is no effective treatment method for improving prognosis.
In addition, in the development of anticancer agents, there are many cases in which development of anticancer agents is forgotten due to clinical failure in the late stage of clinical trials of Phase II and Phase III, for example, Non-Patent Document 3). 1 for this reason is the lack of a model system capable of accurately predicting pharmacological effects. Although the response of cancer to a drug is affected by complex interactions of several factors, including tissue-specific microenvironments, mechanical stimuli, etc., it is very difficult to assess these effects in conventional two-dimensionally cultured cells. Therefore, it is desired to develop a model system which reproduces a disease, especially a disease model having a three-dimensional structure, which is useful for elucidating biological mechanisms of diseases such as cancer and fibrosis, and can predict therapeutic effects on the disease more accurately.
Incidentally, in the field of transplantation, there is a great expectation toward a decellularized organ in which a decellularized organ skeleton is decellularized by its own cell. Decellularized tissue skeletons are relatively easily obtained from tissues and organs of animals and humans, and therefore are widely used as medical materials in practical clinical practice. Biological valves (HANCOK II (R), PERIMOUNT Magna (R), human biological valve (Synegraft) (R)) and the like derived from pig or cow are used as the medical material in the cardiovascular surgery area, Human derived skin (AlloDerm (®)), pig small intestine (OASIS (®)), artificial bone (AlloCraft C-Ring (®)), and the like are used in the area of the orthopedic surgery. Engraftment of "autologous cells" to these medical materials used in clinical theory makes it possible to create autologous organs from other types of organs. (, for example, Non-Patent Document 4), has been reported as a method for engraftment of a self cell or the like, a method for engraftment of a self cell or the like by engraftment of the self cell to the organ on decellularization of the organ to produce a recellular organ. However, as long as the inventors know, it has not been reported that a disease model could be produced from a recellular organ.
  • 出願人(英語)
  • ※2012年7月以前掲載分については米国以外のすべての指定国
  • NAGASAKI UNIVERSITY
  • 発明者(英語)
  • TSUCHIYA, Tomoshi
  • NAGAYASU, Takeshi
  • MIZOGUCHI, Satoshi
国際特許分類(IPC)
指定国 National States: AE AG AL AM AO AT AU AZ BA BB BG BH BN BR BW BY BZ CA CH CL CN CO CR CU CZ DE DJ DK DM DO DZ EC EE EG ES FI GB GD GE GH GM GT HN HR HU ID IL IN IR IS JO JP KE KG KH KN KP KR KW KZ LA LC LK LR LS LU LY MA MD ME MG MK MN MW MX MY MZ NA NG NI NO NZ OM PA PE PG PH PL PT QA RO RS RU RW SA SC SD SE SG SK SL ST SV SY TH TJ TM TN TR TT TZ UA UG US UZ VC VN WS ZA ZM ZW
ARIPO: BW GH GM KE LR LS MW MZ NA RW SD SL SZ TZ UG ZM ZW
EAPO: AM AZ BY KG KZ RU TJ TM
EPO: AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR
OAPI: BF BJ CF CG CI CM GA GN GQ GW KM ML MR NE SN ST TD TG
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