C-26
歷史
最初於1975年分離自一個6個月大的雌性Balb/c實驗小鼠的結腸雜種瘤組織,研究人員通過在腸上單次應用N-亞硝基-N-甲基尿素誘導小鼠形成腫瘤來建立C-26腫瘤細胞模型[1],直至1988年才正式在體外培養中建立C-26細胞系[2],並且發現C-26細胞具有很高的致瘤性及低的轉移趨勢,而接種C-26細胞的小鼠出現高死亡率的情況[2]。1990年,有研究人員發現在食物攝入量不變的情況下,進行體內植入C-26細胞的小鼠普遍會減輕體重,同時出現低血糖和分泌過多皮質類固醇的現象。C-26細胞不僅會使肝功能出現紊亂,還會引致脂肪、骨骼及肌肉組織的損失,因此是研究惡病體質潛在機制的合適模型。值得注意的是C-26細胞誘導的惡病體質會因接種部位的不同而存在差異[3]。近年,有研究人員在小鼠的側面或背部植入C-26腫瘤細胞的固體片段至體內[4]。
科研用途
參考資料
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外部連結
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