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微环境和血管解剖结构对乳腺肿瘤“转移”定植潜能的影响。

Influence of microenvironment and vascular anatomy on "metastatic" colonization potential of mammary tumors.

作者信息

Tarin D, Price J E

出版信息

Cancer Res. 1981 Sep;41(9 Pt 1):3604-9.

PMID:7196284
Abstract

This communication reports experiments demonstrating that some sites in which tumor cells lodge reproducibly fail to support secondary colony formation by a particular tumor, even though cells from the same tumor are already proven to have high colonization potential in other organs. The effect is not an expression of nonspecific hostility to tumor growth, since cells from certain other tumors readily colonize the same site. Cell suspensions obtained by disaggregation of a series of naturally occurring murine mammary tumors were each inoculated by four different routes into separate batches of syngeneic animals, and the resulting degree and distribution of colonization were studied 90 days later at autopsy. Standard doses of 1 million viable tumor cells were injected either i.p. or s.c. into the tail vein or the hepatic portal vein. It was found that some tumors could reproducibly colonize by all routes, whereas others could colonize only by a few, and the combination of sites colonized varied from tumor to tumor; still others were unable to grow in any site. Cells from nonneoplastic lactating mammary glands did not establish any colonies. We have demonstrated previously that individual naturally occurring mammary tumors differ in their pulmonary colonization potentials after i.v. inoculation and that the potential of a given tumor is an intrinsic property of its constituent cells. The current findings are evidence that the microenvironment of an organ can inhibit or permit expression of this intrinsic potential and that the degree and sites of colonization are thus the results of interaction between tumor and organ-specific factors. It was also found that circulatory anatomy partially influenced the distribution of colonies and that colonization of distant organs after blood-borne dissemination is distinct from general tumor transplantability.

摘要

本通讯报道了一些实验,这些实验表明,某些肿瘤细胞可重复性地定植的部位,却无法支持特定肿瘤形成继发性集落,尽管同一肿瘤的细胞已被证明在其他器官中具有很高的定植潜力。这种效应并非对肿瘤生长的非特异性敌意的表现,因为来自某些其他肿瘤的细胞很容易在同一部位定植。通过解离一系列自然发生的小鼠乳腺肿瘤获得的细胞悬液,分别通过四种不同途径接种到同基因动物的不同批次中,并在90天后尸检时研究由此产生的定植程度和分布。将100万个活肿瘤细胞的标准剂量通过腹腔内、皮下、尾静脉或肝门静脉注射。结果发现,一些肿瘤可以通过所有途径可重复性地定植,而另一些肿瘤只能通过少数途径定植,并且定植部位的组合因肿瘤而异;还有一些肿瘤在任何部位都无法生长。来自非肿瘤性泌乳乳腺的细胞没有形成任何集落。我们之前已经证明,个体自然发生的乳腺肿瘤在静脉注射后的肺定植潜力不同,并且给定肿瘤的潜力是其组成细胞的固有特性。目前的研究结果证明,器官的微环境可以抑制或允许这种固有潜力的表达,因此定植的程度和部位是肿瘤与器官特异性因素相互作用的结果。还发现循环解剖结构部分影响集落的分布,并且血行播散后远处器官的定植与一般肿瘤移植性不同。

相似文献

1
Influence of microenvironment and vascular anatomy on "metastatic" colonization potential of mammary tumors.微环境和血管解剖结构对乳腺肿瘤“转移”定植潜能的影响。
Cancer Res. 1981 Sep;41(9 Pt 1):3604-9.
2
Analysis of organ-specific effects on metastatic tumor formation by studies in vitro.通过体外研究分析器官特异性对转移性肿瘤形成的影响。
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Severe combined immunodeficient-hu model of human prostate cancer metastasis to human bone.人前列腺癌转移至人骨的严重联合免疫缺陷-人模型
Cancer Res. 1999 Apr 15;59(8):1987-93.
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Clonogenicity and experimental metastatic potential of spontaneous mouse mammary neoplasms.自发性小鼠乳腺肿瘤的克隆形成能力及实验性转移潜能
J Natl Cancer Inst. 1986 Aug;77(2):529-35.
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In vivo isolation of a metastatic tumor cell variant involving selective and nonadaptive processes.通过体内方法分离出一种涉及选择性和非适应性过程的转移性肿瘤细胞变体。
J Natl Cancer Inst. 1981 Jan;66(1):183-9.
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Tumor cell dissemination patterns and metastasis of murine mammary carcinoma.
Cancer Res. 1989 Feb 1;49(3):570-5.
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Spontaneous and induced metastasis of naturally occurring tumors in mice: analysis of cell shedding into the blood.小鼠自然发生肿瘤的自发和诱导转移:对进入血液的细胞脱落的分析。
J Natl Cancer Inst. 1984 Dec;73(6):1319-26.
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Experimental analysis of factors affecting metastatic spread using naturally occurring tumours.利用自然发生的肿瘤对影响转移扩散因素的实验分析
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Organ preferences in metastatic colony formation by spontaneous mammary carcinomas after intra-arterial inoculation.动脉内接种后自发性乳腺癌转移瘤形成中的器官偏好性
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Metastatic behavior of a murine reticulum cell sarcoma exhibiting organ-specific growth.表现出器官特异性生长的小鼠网状细胞肉瘤的转移行为。
Cancer Res. 1981 Apr;41(4):1281-7.

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