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将仓鼠黑色素瘤移植到无胸腺小鼠体内后的生长与转移情况。

Growth and metastasis of hamster melanoma following transplantation into athymic mice.

作者信息

Schleicher R L, Green A W, Beattie C W

出版信息

Cancer Res. 1987 Aug 15;47(16):4465-70.

PMID:3607776
Abstract

Melanotic hamster malignant melanoma (MM1) is a transplantable, locally invasive tumor which metastasizes widely in syngeneic hosts. We have established three clones, HM1, HM3, and HM4 of the original MM1 line in culture. Inoculation (s.c.) into 4- to 5-week-old male athymic mice produced highly vascular, melanotic, locally invasive tumors in 100% of mice inoculated with a latency of 4-7 days. Karyotype analysis of HM cells revealed modal chromosome numbers of 39-41 (43% HM1), 43 (22% HM3), and 44-47 (61% HM4). Sixty-one % of HM1 cells were hypodiploid, 4% diploid, and 5% hyperdiploid. HM1, -3, and -4 cells also exhibited aneuploidy, endoreduplication, translocational exchanges, additions, deletions, dicentromeric and ring chromosomes, and double minutes although not all cells exhibited all abnormalities. Initial metastasis was to regional lymph nodes with eventual progression to lung and liver. Mice inoculated with HM1, -3, and -4 cells were dead with metastatic disease within 57, 63, and 64 days, respectively, following s.c. inoculation (5 X 10(5) cells) when the mice were 90-100 days old. Mortality rate was highest in line HM3 with 50% of the mice dead within 33 days postinoculation. Metastatic potential of HM1 and HM3 cells rose significantly when successive generations of HM1 and HM3 cells cultured from isolated lung metastasis were reinoculated. Metastasis to lymph nodes and liver was not observed with increasing passage generations of lung metastasis. Our observations provide evidence that hamster melanomas are clonally heterogenous, locally invasive, and exhibit rapid growth and metastasis following s.c. inoculation into adult athymic mice. Transplantable melanotic hamster melanoma cells also exhibit a significant preferential metastasis to lung following culture and sequential reinoculation of lung metastasis in athymic mice. As such, they appear to provide a reproducible model of metastasis in an immunocompromised host.

摘要

黑色素瘤仓鼠恶性黑色素瘤(MM1)是一种可移植的局部侵袭性肿瘤,在同基因宿主中广泛转移。我们已经在培养物中建立了原始MM1细胞系的三个克隆,即HM1、HM3和HM4。将其皮下接种到4至5周龄的雄性无胸腺小鼠中,100%的接种小鼠在4至7天的潜伏期后产生了高度血管化、黑色素化的局部侵袭性肿瘤。对HM细胞的核型分析显示,HM1细胞的众数染色体数为39 - 41(43%),HM3为43(22%),HM4为44 - 47(61%)。61%的HM1细胞为亚二倍体,4%为二倍体,5%为超二倍体。HM1、HM3和HM4细胞还表现出非整倍体、核内复制、易位交换、添加、缺失、双着丝粒和环状染色体以及双微体,尽管并非所有细胞都表现出所有这些异常。最初转移至局部淋巴结,最终进展至肺和肝。皮下接种(5×10⁵个细胞)HM1、HM3和HM4细胞的小鼠,在90 - 100日龄时,分别在接种后57、63和64天死于转移性疾病。HM3细胞系的死亡率最高,50%的小鼠在接种后33天内死亡。当从分离的肺转移灶培养的HM1和HM3细胞的连续传代细胞再次接种时,HM1和HM3细胞的转移潜能显著升高。随着肺转移灶传代次数的增加,未观察到向淋巴结和肝的转移。我们的观察结果提供了证据,表明仓鼠黑色素瘤具有克隆异质性、局部侵袭性,并且在皮下接种到成年无胸腺小鼠后表现出快速生长和转移。可移植的黑色素瘤仓鼠黑色素瘤细胞在无胸腺小鼠中培养并依次接种肺转移灶后,也表现出对肺的显著优先转移。因此,它们似乎提供了一种在免疫受损宿主中可重复的转移模型。

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