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肿瘤球体中增殖-侵袭转化的形态定量。

Morphological quantification of proliferation-to-invasion transition in tumor spheroids.

机构信息

Chongqing Key Laboratory of Soft Condensed Matter Physics and Smart Materials, College of Physics, Chongqing University, Chongqing 401331, China.

Department of Physics, Xiamen University, Xiamen 361005, China.

出版信息

Biochim Biophys Acta Gen Subj. 2020 Jan;1864(1):129460. doi: 10.1016/j.bbagen.2019.129460. Epub 2019 Oct 28.

Abstract

BACKGROUND

Metastasis determines the lethality of cancer. In most clinical cases, patients are able to live with tumor proliferation before metastasis. Thus, the transition from tumor proliferation to metastasis/invasion is essential. However, the mechanism is still unclear and especially, the proliferation-to-metastasis/invasion transition point has not been well defined. Therefore, quantitative characterization of this transition is urgently needed.

METHODS

We have successfully developed a home-built living-cell incubation system combined with an inverted optical microscope, and a systematic, quantitative approach to describing the major characteristic morphological parameters for the identification of the critical transition points for tumor-cell spheroids in a collagen fiber scaffold.

RESULTS

The system focuses on in vitro tumor modeling, e.g. the development of tumor-cell spheroids in a collagen fiber scaffold and the monitoring of cell transition from proliferation to invasion. By applying this approach to multiple tumor spheroid models, such as U87 (glioma tumor), H1299 (lung cancer), and MDA-MB-231 (breast cancer) cells, we have obtained quantitative morphological references to evaluate the proliferation-to-invasion transition time, as well as differentiating the invasion potential of tumor cells upon environmental changes, i.e. drug application.

CONCLUSIONS

Our quantitative approach provides a feasible clarification for the proliferation-to-invasion transition of in vitro tumor models (spheroids). Moreover, the transition time is a useful reference for the invasive potential of tumor cells.

GENERAL SIGNIFICANCE

This quantitative approach is potentially applicable to primary tumor cells, and thus has potential applications in the fields of cancer metastasis investigations and clinical diagnostics.

摘要

背景

转移决定了癌症的致命性。在大多数临床情况下,患者在转移前能够耐受肿瘤的增殖。因此,从肿瘤增殖到转移/浸润的转变是至关重要的。然而,其机制仍不清楚,特别是增殖到转移/浸润的转变点尚未得到很好的定义。因此,迫切需要对这一转变进行定量描述。

方法

我们成功地开发了一种内置的活细胞孵育系统,结合倒置光学显微镜,以及一种系统的、定量的方法来描述主要的形态特征参数,以识别肿瘤细胞球在胶原纤维支架中的关键转变点。

结果

该系统专注于体外肿瘤建模,例如肿瘤细胞球在胶原纤维支架中的发展和细胞从增殖到侵袭的转变监测。通过将这种方法应用于多个肿瘤球模型,如 U87(神经胶质瘤肿瘤)、H1299(肺癌)和 MDA-MB-231(乳腺癌)细胞,我们获得了定量的形态学参考,以评估增殖到侵袭的转变时间,并区分肿瘤细胞在环境变化(如药物应用)下的侵袭潜力。

结论

我们的定量方法为体外肿瘤模型(球体)的增殖到侵袭转变提供了可行的解释。此外,转变时间是肿瘤细胞侵袭潜力的有用参考。

意义

这种定量方法可能适用于原发性肿瘤细胞,因此在癌症转移研究和临床诊断领域具有潜在的应用价值。

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