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培养的人肺癌细胞谱:一种研究肿瘤进展和转移分子决定因素的潜在模型。

The spectrum of human lung cancer cells in culture: a potential model for studying molecular determinants of tumor progression and metastasis.

作者信息

Baylin S B, Jackson R H, Lennarz W, Shaper J H

出版信息

Symp Fundam Cancer Res. 1983;36:281-91.

PMID:6089293
Abstract

We have reviewed the behavior of human lung cancer cells in culture. We have considered the implications of cell biology and biochemistry studies of the cultured cells for the in vivo behavior of lung neoplasms, including the metastatic potential of the different tumor types. Among the human lung cancers, SCC, which grows in culture as suspended aggregates of adherent cells, metastasizes earlier in the life cycle of the tumor and more widely than the major types of non-SCC lung cancers. These latter tumors grow as anchorage-dependent cells in culture. We have pointed out that ultrastructural studies of cultured human lung cancer cells reveal dramatic changes in cell surface membrane morphology coincident with progressive loss of SCC features and intercellular adhesion. We have stressed the potential value of these cultures of human lung cancer cells for studying the molecular determinants of intercellular adhesion and their importance to the process of metastasis. In this context, we have stressed that a different cell surface protein phenotype exists between SCC and non-SCC lung cancer cells in culture and that some of these proteins could be intimately involved in the different growth behavior patterns of these tumor cells. Finally, we have pointed out the need to construct models in which the growth characteristics and biochemical properties of cultured lung cancer cells can be directly compared in vivo with their metastatic potential.

摘要

我们回顾了培养的人肺癌细胞的行为。我们考虑了对培养细胞进行细胞生物学和生物化学研究对于肺肿瘤体内行为的意义,包括不同肿瘤类型的转移潜能。在人类肺癌中,鳞状细胞癌(SCC)在培养时以贴壁细胞的悬浮聚集体形式生长,在肿瘤生命周期中比主要类型的非SCC肺癌更早且更广泛地发生转移。后一种肿瘤在培养时作为锚定依赖性细胞生长。我们指出,对培养的人肺癌细胞的超微结构研究显示,细胞表面膜形态发生了显著变化,这与SCC特征和细胞间粘附的逐渐丧失相一致。我们强调了这些人肺癌细胞培养物对于研究细胞间粘附的分子决定因素及其对转移过程的重要性的潜在价值。在此背景下,我们强调在培养的SCC和非SCC肺癌细胞之间存在不同的细胞表面蛋白表型,并且其中一些蛋白可能与这些肿瘤细胞的不同生长行为模式密切相关。最后,我们指出需要构建模型,以便能够在体内直接比较培养的肺癌细胞的生长特征和生化特性与其转移潜能。

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