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Erschienen in: Medical Oncology 3/2014

01.03.2014 | Original Paper

Alterations in mechanical properties are associated with prostate cancer progression

verfasst von: Xuejian Wang, Jianbo Wang, Yingxi Liu, Huafeng Zong, Xiangyu Che, Wei Zheng, Feng Chen, Zheng Zhu, Deyong Yang, Xishuang Song

Erschienen in: Medical Oncology | Ausgabe 3/2014

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Abstract

Cancer progression and metastasis have been shown to be accompanied by alterations in the mechanical properties of tissues, but the relationship between the mechanical properties and malignant behavior in prostate cancer (Pca) is less clear. The aims of this study were to detect the mechanical properties of benign prostatic hyperplasia (BPH) and Pca tissues on both the macro- and micro-scales, to explore the relationships between mechanical properties and malignant behavior and, finally, to identify the important molecules in the mechanotransduction signaling pathway. We demonstrated that the strain index of Pca tissue was significantly higher than that of BPH tissue on the macro-scale but the Young’s modulus of the Pca tissues, especially in advanced Pca, was lower than that of BPH tissues on the micro-scale. These two seemingly contradictory results can be explained by the excessive proliferation of tumor cells (Ki-67) and the degradation of scaffold proteins (collagens). These data indicate that alterations of the macro- and micro-mechanical properties of Pca tissues with malignant behavior are contradictory. The mechanical properties of tissues might be useful as a new risk factor for malignancy and metastasis in Pca. Furthermore, collagens, matrix metalloproteinase, fibronectin, and integrins might be the important molecules in the mechanotransduction signaling pathway.
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Metadaten
Titel
Alterations in mechanical properties are associated with prostate cancer progression
verfasst von
Xuejian Wang
Jianbo Wang
Yingxi Liu
Huafeng Zong
Xiangyu Che
Wei Zheng
Feng Chen
Zheng Zhu
Deyong Yang
Xishuang Song
Publikationsdatum
01.03.2014
Verlag
Springer US
Erschienen in
Medical Oncology / Ausgabe 3/2014
Print ISSN: 1357-0560
Elektronische ISSN: 1559-131X
DOI
https://doi.org/10.1007/s12032-014-0876-9

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