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一种新的人乳腺癌细胞系KPL-3C,可分泌甲状旁腺激素相关蛋白,并在裸鼠体内产生与微钙化相关的肿瘤。

A new human breast cancer cell line, KPL-3C, secretes parathyroid hormone-related protein and produces tumours associated with microcalcifications in nude mice.

作者信息

Kurebayashi J, Kurosumi M, Sonoo H

机构信息

Department of Endocrine Surgery, Kawasaki Medical School, Okayama, Japan.

出版信息

Br J Cancer. 1996 Jul;74(2):200-7. doi: 10.1038/bjc.1996.338.

Abstract

Parathyroid hormone-related protein (PTHrP) is the main cause of humoral hypercalcaemia of malignancy (HHM). We recently established a new human breast cancer cell line, designated KPL-3C, from the malignant effusion of a breast cancer patient with HHM. Morphological, cytogenetic and immunohistochemical analyses indicated that the cell line is derived from human breast cancer. The KPL-3C cells stably secrete immunoreactive PTHrP measured by a two-site immunoradiometric assay, possess both oestrogen and progesterone receptors and are tumorigenic in female nude mice. The addition of phorbol-12-myristate-13-acetate to the medium significantly increased PTHrP secretion from the cells. In contrast, hydrocortisone, medroxyprogesterone acetate and 22-oxacalcitriol decreased PTHrP secretion in a dose-dependent manner. Unexpectedly, a number of microcalcifications were observed in the transplanted tumours. Radiographical examination indicated that the microcalcifications in the tumours are very similar to those commonly observed in human breast cancer. These findings suggest that this KPL-3C cell line may be useful for studying the regulatory mechanisms of PTHrP secretion and the mechanisms that lead to the deposition of microcalcifications in breast cancer.

摘要

甲状旁腺激素相关蛋白(PTHrP)是恶性肿瘤体液性高钙血症(HHM)的主要病因。我们最近从一名患有HHM的乳腺癌患者的恶性胸腔积液中建立了一种新的人乳腺癌细胞系,命名为KPL-3C。形态学、细胞遗传学和免疫组织化学分析表明,该细胞系源自人乳腺癌。通过双位点免疫放射分析测定,KPL-3C细胞稳定分泌免疫反应性PTHrP,同时具有雌激素和孕激素受体,并且在雌性裸鼠中具有致瘤性。向培养基中添加佛波醇-12-肉豆蔻酸酯-13-乙酸盐可显著增加细胞中PTHrP的分泌。相反,氢化可的松、醋酸甲羟孕酮和22-氧杂骨化三醇以剂量依赖的方式降低PTHrP的分泌。出乎意料的是,在移植瘤中观察到了一些微钙化。影像学检查表明,肿瘤中的微钙化与人类乳腺癌中常见的微钙化非常相似。这些发现表明,这种KPL-3C细胞系可能有助于研究PTHrP分泌的调节机制以及导致乳腺癌中微钙化沉积的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113a/2074563/98c4fe531cf0/brjcancer00018-0042-a.jpg

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