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硫化镍诱导恶性肿瘤的机制。

The mechanism of malignant tumor induction by nickel subsulfide.

作者信息

Lumb G, Sunderman F W

机构信息

Department of Pathology, Hahnemann University College of Medicine, Philadelphia, PA 19102.

出版信息

Ann Clin Lab Sci. 1988 Sep-Oct;18(5):353-66.

PMID:2460016
Abstract

Experiments were performed to study the earliest changes and their sequence in the development of malignant tumors following implantation of 10 mg of nickel subsulfide (Ni3S2) into the right quadriceps muscle of seven male Fischer rats. Biopsies were performed when nodules reached one to three mm, and, later, when they were five to seven mm, and, finally, at sacrifice, to confirm the fully developed tumor pattern. Light microscopy of the earliest samples showed groups of cells clumped and scattered among degenerating muscle fibers. Mitoses were seen and inflammatory cells were not a feature. Electron microscopy showed individual degenerating muscle fibers, but also cells with characteristic features of myofibroblasts. In many cells osmium, dense fragments suggestive of crystalline material, were seen in the cytoplasm and nuclei. In the second set of biopsy material, myofibroblasts with well defined and dilated rough endoplasmic reticulum, intracellular membrane-bound collagen, and microfilaments with focal "dense bodies" were numerous. Mitoses were frequent. Immunohistochemistry showed strongly positive reaction to Vimentin and muscle-specific Actin in the tumor cells. In the fully developed tumors, the previously described typical storiform cell pattern with spindle and spheroidal cells with frequent mitoses was seen. Vimentin and muscle-specific Actin stains were strongly positive. The long latent period, the evidence of cell degeneration, necrosis, foreign material (probably of nickel composition), cell invasion, and subsequent rapid myofibroblast-type cell development, proliferating to malignant tumors highly suggestive of malignant fibrous histiocytoma, seem to suggest an epigenetic form of carcinogenicity of cytotoxic variety. Whether the tumor cells derive from transformed myofibrils or from activated pluripotential mesenchymal cells, or from both, remains in doubt.

摘要

实验旨在研究将10毫克硫化镍(Ni3S2)植入7只雄性Fischer大鼠右股四头肌后,恶性肿瘤发生发展过程中最早出现的变化及其顺序。当结节达到1至3毫米时进行活检,之后结节达到5至7毫米时再次活检,最后在处死时进行活检,以确认肿瘤的完全发展模式。最早样本的光学显微镜检查显示,细胞群聚集并散布在退变的肌纤维之间。可见有丝分裂,且无炎症细胞。电子显微镜检查显示有个别退变的肌纤维,但也有具有肌成纤维细胞特征性的细胞。在许多细胞的细胞质和细胞核中可见锇,有提示晶体物质的致密碎片。在第二组活检材料中,有大量肌成纤维细胞,其粗面内质网清晰且扩张,有细胞内膜结合的胶原蛋白,还有带有局灶性“致密小体”的微丝。有丝分裂频繁。免疫组织化学显示肿瘤细胞对波形蛋白和肌肉特异性肌动蛋白呈强阳性反应。在完全发展的肿瘤中,可见先前描述的典型席纹状细胞模式,有梭形细胞和球形细胞,有频繁的有丝分裂。波形蛋白和肌肉特异性肌动蛋白染色呈强阳性。较长的潜伏期、细胞退变、坏死、异物(可能是镍成分)、细胞侵袭以及随后快速的肌成纤维细胞样细胞发展并增殖为高度提示恶性纤维组织细胞瘤的恶性肿瘤,似乎提示了一种细胞毒性类型致癌性的表观遗传形式。肿瘤细胞是源自转化的肌原纤维还是活化的多能间充质细胞,或者两者皆有,仍不确定。

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