Verbruggen Anneke S K, McCarthy Elan C, Dwyer Roisin M, McNamara Laoise M
Mechanobiology and Medical Device Research group (MMDRG), Biomedical Engineering, College of Science and Engineering, National University of Ireland Galway, Ireland.
Discipline of Surgery, Lambe Institute for Translational Research, National University of Ireland Galway, Ireland.
Bone Rep. 2022 Jun 12;17:101597. doi: 10.1016/j.bonr.2022.101597. eCollection 2022 Dec.
Cancer cells favour migration and metastasis to bone tissue for 70-80 % of advanced breast cancer patients and it has been proposed that bone tissue provides attractive physical properties that facilitate tumour invasion, resulting in osteolytic and or osteoblastic metastasis. However, it is not yet known how specific bone tissue composition is associated with tumour invasion. In particular, how compositional and nano-mechanical properties of bone tissue evolve during metastasis, and where in the bone they arise, may affect the overall aggressiveness of tumour invasion, but this is not well understood. The objective of this study is to develop an advanced understanding of temporal and spatial changes in nano-mechanical properties and composition of bone tissue during metastasis. Primary mammary tumours were induced by inoculation of immune-competent BALB/c mice with 4T1 breast cancer cells in the mammary fat pad local to the right femur. Microcomputed tomography and nanoindentation were conducted to quantify cortical and trabecular bone matrix mineralisation and nano-mechanical properties. Analysis was performed in proximal and distal femur regions (spatial analysis) of tumour-adjacent (ipsilateral) and contralateral femurs after 3 weeks and 6 weeks of tumour and metastasis development (temporal analysis). By 3 weeks post-inoculation there was no significant difference in bone volume fraction or nano-mechanical properties of bone tissue between the metastatic femora and healthy controls. However, early osteolysis was indicated by trabecular thinning in the distal and proximal trabecular compartment of tumour-bearing femora. Moreover, cortical thickness was significantly increased in the distal region, and the mean mineral density was significantly higher in cortical and trabecular bone tissue in both proximal and distal regions, of ipsilateral (tumour-bearing) femurs compared to healthy controls. By 6 weeks post-inoculation, overt osteolytic lesions were identified in all ipsilateral metastatic femora, but also in two of four contralateral femora of tumour-bearing mice. Bone volume fraction, cortical area, cortical and trabecular thickness were all significantly decreased in metastatic femora (both ipsilateral and contralateral). Trabecular bone tissue stiffness in the proximal femur decreased in the ipsilateral femurs compared to contralateral and control sites. Temporal and spatial analysis of bone nano-mechanical properties and mineralisation during breast cancer invasion reveals changes in bone tissue composition prior to and following overt metastatic osteolysis, local and distant from the primary tumour site. These changes may alter the mechanical environment of both the bone and tumour cells, and thereby play a role in perpetuating the cancer vicious cycle during breast cancer metastasis to bone tissue.
对于70 - 80%的晚期乳腺癌患者而言,癌细胞倾向于迁移并转移至骨组织。有人提出,骨组织具有吸引人的物理特性,有助于肿瘤侵袭,从而导致溶骨性和成骨性转移。然而,目前尚不清楚骨组织的具体组成如何与肿瘤侵袭相关联。特别是,骨组织的组成和纳米力学特性在转移过程中如何演变,以及它们在骨中的何处出现,可能会影响肿瘤侵袭的整体侵袭性,但对此尚未得到充分理解。本研究的目的是深入了解转移过程中骨组织纳米力学特性和组成的时空变化。通过将免疫活性BALB/c小鼠的乳腺脂肪垫(位于右股骨局部)接种4T1乳腺癌细胞来诱导原发性乳腺肿瘤。进行微型计算机断层扫描和纳米压痕以量化皮质骨和小梁骨基质矿化及纳米力学特性。在肿瘤和转移发展3周和6周后,对肿瘤相邻(同侧)和对侧股骨的近端和远端股骨区域进行分析(空间分析)。接种后3周,转移股骨与健康对照之间的骨体积分数或骨组织的纳米力学特性没有显著差异。然而,在荷瘤股骨的远端和近端小梁区域,小梁变薄表明早期存在溶骨现象。此外,同侧(荷瘤)股骨远端区域的皮质厚度显著增加,与健康对照相比,同侧股骨近端和远端区域的皮质骨和小梁骨组织的平均矿物质密度显著更高。接种后6周,在所有同侧转移股骨中均发现明显的溶骨性病变,但在荷瘤小鼠的四只对侧股骨中有两只也出现了这种情况。转移股骨(同侧和对侧)的骨体积分数、皮质面积、皮质和小梁厚度均显著降低。与对侧和对照部位相比,同侧股骨近端小梁骨组织的硬度降低。乳腺癌侵袭过程中骨纳米力学特性和矿化的时空分析揭示了在明显的转移性溶骨之前和之后,远离原发肿瘤部位的局部和远处骨组织组成的变化。这些变化可能会改变骨和肿瘤细胞的力学环境,从而在乳腺癌转移至骨组织的过程中在维持癌症恶性循环方面发挥作用。