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A novel patient-derived orthotopic xenograft (PDOX) mouse model of highly-aggressive liver metastasis for identification of candidate effective drug-combinations

机译:一种新型患者衍生的原位异种移植(PDOX)小鼠模型的高侵袭性肝转移,用于鉴定候选有效药物组合

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Liver metastasis is a recalcitrant disease that usually leads to death of the patient. The present study established a unique patient-derived orthotopic xenograft (PDOX) nude mouse model of a highly aggressive liver metastasis of colon cancer. The aim of the present study was to demonstrate proof-of-concept that candidate drug combinations could significantly inhibit growth and re-metastasis of this recalcitrant tumor. The patient’s liver metastasis was initially established subcutaneously in nude mice and the subcutaneous tumor tissue was then orthotopically implanted in the liver of nude mice to establish a PDOX model. Two studies were performed to test different drugs or drug combination, indicating that 5-fluorouracil (5-FU)?+?irinotecan (IRI)?+?bevacizumab (BEV) and regorafenib (REG)?+?selumetinib (SEL) had significantly inhibited liver metastasis growth (p?=?0.013 and p?=?0.035, respectively), and prevented liver satellite metastasis. This study is proof of concept that a PDOX model of highly aggressive colon-cancer metastasis can identify effective drug combinations and that the model has future clinical potential.
机译:肝转移是一种通常导致患者死亡的顽皮症疾病。本研究建立了一种独特的患者衍生的原位异种移植(PDOX)裸鼠裸鼠模型的结肠癌的肝脏转移。本研究的目的是证明概念证明,候选药物组合可以显着抑制这种顽抗肿瘤的生长和再转移。患者的肝脏转移最初在裸鼠中皮下来,然后在裸鼠的肝脏中纯化肿瘤组织,以建立PDOX模型。进行两项研究以测试不同的药物或药物组合,表明5-氟尿嘧啶(5-FU)?+?伊替康(IRI)?+?BEVACIZUMAB(BEV)和RegoraFenib(REG)?+?SELUMETINIB(SEL)显着抑制肝转移生长(p?=Δ= 0.013和p?= 0.035),并防止肝脏卫星转移。本研究证明了概念,即高侵袭性结肠癌转移的PDOX模型可以识别有效的药物组合,并且该模型具有未来的临床潜力。

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