Shimosato Y, Kameya T, Hirohashi S
Pathol Annu. 1979;14 Pt 2:215-57.
Tansplantability, growth, morphology, and function of xenotransplanted human tumors, such as carcinomas of the lung, liver, breast, choriocarcinoma, and blastomas of the liver, lung, kidney, and uterus, are described. From the tumor take rate, it is clear that xenotransplantation cannot be used for the study of every human tumor: slow-growing tumors are difficult to analyze, and functioning adenomas and low-grade malignant carcinomas are at present almost impossible to study by this approach. From the authors' transplantation experience, tumor antigenicity to nude mice with no T-cell function, either tumor specific or species specific, was suspected. Therefore, the growth in nude mice may not equate to that in the human body. The stroma of the transplanted tumor, which is most likely of mouse origin, might also alter the growth rate, as it did the histology of some tumors. Another possible hindrance that has not been described in the text is the mouse endogenous virus. Serially transplanted human tumors are often infected with C particles, which could well influence the tumor growth and character. In spite of the presence of some factors unfavorable for the study of human tumors through xenotransplantation, it has, nevertheless, been clearly shown that the nude mouse/human tumor system is a very useful tool for functional analysis of tumors in relation to growth, differentiation, and morphology, such as eutopic or ectopic production of various hormones, AFP, normal serum proteins, colony-stimulating factor, erythropoietin, and so on. This system can be employed to elucidate the production of many other biologically active and inactive substances by a variety of tumors and their effects on the host in the future and should provide better understanding of human cancers. Attempts to induce differentiation and to change the biologic behavior of xenotransplanted human malignant tumors have failed so far, except for induced dormancy of breast carcinoma under unfavorable hormonal conditions. This line of investigation may have particular import on cancer research, particularly in relation to the biology and treatment of human cancers.
本文描述了异种移植的人类肿瘤,如肺癌、肝癌、乳腺癌、绒毛膜癌以及肝、肺、肾和子宫的母细胞瘤的移植性、生长情况、形态和功能。从肿瘤接种率来看,很明显异种移植不能用于研究所有人类肿瘤:生长缓慢的肿瘤难以分析,功能性腺瘤和低级别恶性癌目前几乎无法通过这种方法进行研究。根据作者的移植经验,怀疑对无T细胞功能的裸鼠存在肿瘤抗原性,无论是肿瘤特异性还是物种特异性。因此,裸鼠体内的生长情况可能与人体情况不同。移植肿瘤的基质很可能来源于小鼠,这也可能改变生长速度,就像它对一些肿瘤的组织学产生影响一样。文中未提及的另一个可能的障碍是小鼠内源性病毒。连续移植的人类肿瘤常感染C颗粒,这很可能会影响肿瘤的生长和特征。尽管存在一些不利于通过异种移植研究人类肿瘤的因素,但裸鼠/人类肿瘤系统已被清楚地证明是一种非常有用的工具,可用于对肿瘤的生长、分化和形态进行功能分析,例如各种激素、甲胎蛋白、正常血清蛋白、集落刺激因子、促红细胞生成素等的原位或异位产生。该系统未来可用于阐明多种肿瘤产生的许多其他生物活性和非活性物质及其对宿主的影响,并应能更好地理解人类癌症。到目前为止,除了在不利的激素条件下诱导乳腺癌休眠外,诱导异种移植的人类恶性肿瘤分化和改变其生物学行为的尝试均告失败。这一系列研究可能对癌症研究具有特殊意义,特别是在人类癌症的生物学和治疗方面。