Morphomechanical and structural changes induced by ROCK inhibitor in breast cancer cells

被引:31
作者
Cascione, Mariafrancesca [1 ]
De Matteis, Valeria [2 ]
Toma, Chiara Cristina [2 ]
Pellegrino, Paolo [2 ]
Leporatti, Stefano [3 ]
Rinaldi, Rosaria [2 ]
机构
[1] Univ Bari Aldo Moro, Policlin Bari, Dipartimento Sci Biomed & Oncol Umana, Bari, Italy
[2] Univ Salento, Dipartimento Matemat & Fis E De Giorgi, Via Monteroni, I-73100 Lecce, Italy
[3] CNR, Nanotec Ist Nanotecnol, Polo Nanotecnol, Campus Ecoteckne, Lecce, Italy
关键词
ROCK; Y-27632; Biomechanical properties; Cancer cells; AFM; EPITHELIAL-MESENCHYMAL TRANSITIONS; ATOMIC-FORCE MICROSCOPY; RHO-KINASE; ACTIN CYTOSKELETON; Y-27632; GTPASES; PROGRESSION; METASTASIS; MECHANICS; CARCINOMA;
D O I
10.1016/j.yexcr.2017.09.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The EMT phenomenon is based on tumour progression. The cells lose their physiologic phenotype and assumed a mesenchymal phenotype characterized by an increased migratory capacity, invasiveness and high resistance to apoptosis. In this process, RHO family regulates the activation or suppression of ROCK (Rho-associated coiled coil containing protein kinase) which in turn regulates the cytoskeleton dynamics. However, while the biochemical mechanisms are widely investigated, a comprehensive and careful estimation of biomechanical changes has not been extensively addressed. In this work, we used a strong ROCK inhibitor, Y-27632, to evaluate the effects of inhibition on living breast cancer epithelial cells by a biomechanical approach. Atomic Force Microscopy (AFM) was used to estimate changes of cellular elasticity, quantified by Young's modulus parameter. The morphometric alterations were analyzed by AFM topographies and Confocal Laser Scanning Microscopy (CLSM). Our study revealed a significant modification in the Young's modulus after treatment, especially as regards cytoskeletal region. Our evidences suggest that the use of Y-27632 enhanced the cell rigidity, preventing cell migration and arrested the metastasization process representing a potential powerful factor for cancer treatment.
引用
收藏
页码:303 / 309
页数:7
相关论文
共 53 条
[1]   Rho-kinase inhibitor upregulates migration by altering focal adhesion formation via the Akt pathway in colon cancer cells [J].
Adachi, Seiji ;
Yasuda, Ichiro ;
Nakashima, Masanori ;
Yamauchi, Takahiro ;
Yoshioka, Takashi ;
Okano, Yukio ;
Moriwaki, Hisataka ;
Kozawa, Osamu .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2011, 650 (01) :145-150
[2]   A Proteomic Approach for Comprehensively Screening Substrates of Protein Kinases Such as Rho-Kinase [J].
Amano, Mutsuki ;
Tsumura, Yuta ;
Taki, Kentaro ;
Harada, Hidenori ;
Mori, Kazutaka ;
Nishioka, Tomoki ;
Kato, Katsuhiro ;
Suzuki, Takeshi ;
Nishioka, Yosuke ;
Iwamatsu, Akihiro ;
Kaibuchi, Kozo .
PLOS ONE, 2010, 5 (01)
[3]   Rho GTPases and their effector proteins [J].
Bishop, AL ;
Hall, A .
BIOCHEMICAL JOURNAL, 2000, 348 (02) :241-255
[4]   Hyaluronan-mediated CD44 interaction with RhoGEF and Rho kinase promotes Grb2-associated binder-1 phosphorylation and phosphatidylinositol 3-kinase signaling leading to cytokine (Macrophage-Colony stimulating factor) production and breast tumor progression [J].
Bourguignon, LYW ;
Singleton, PA ;
Zhu, HB ;
Diedrich, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (32) :29420-29434
[5]   CALCULATION OF THERMAL NOISE IN ATOMIC-FORCE MICROSCOPY [J].
BUTT, HJ ;
JASCHKE, M .
NANOTECHNOLOGY, 1995, 6 (01) :1-7
[6]   Atomic Force Microscopy Combined with Optical Microscopy for Cells Investigation [J].
Cascione, Mariafrancesca ;
De Matteis, Valeria ;
Rinaldi, Rosaria ;
Leporatti, Stefano .
MICROSCOPY RESEARCH AND TECHNIQUE, 2017, 80 (01) :109-123
[7]   The nuclear envelope environment and its cancer connections [J].
Chow, Kin-Hoe ;
Factor, Rachel E. ;
Ullman, Katharine S. .
NATURE REVIEWS CANCER, 2012, 12 (03) :196-209
[8]   Genomic analysis of metastasis reveals an essential role for RhoC [J].
Clark, EA ;
Golub, TR ;
Lander, ES ;
Hynes, RO .
NATURE, 2000, 406 (6795) :532-535
[9]   Nanomechanical analysis of cells from cancer patients [J].
Cross, Sarah E. ;
Jin, Yu-Sheng ;
Rao, Jianyu ;
Gimzewski, James K. .
NATURE NANOTECHNOLOGY, 2007, 2 (12) :780-783
[10]   AFM-based analysis of human metastatic cancer cells [J].
Cross, Sarah E. ;
Jin, Yu-Sheng ;
Tondre, Julianne ;
Wong, Roger ;
Rao, JianYu ;
Gimzewski, James K. .
NANOTECHNOLOGY, 2008, 19 (38)