3 Furthermore, once established, Acalabrutinib in vivo tumor development is associated with further increases in matrix stiffness to values greater than those of the surrounding hepatic parenchyma.4 It is therefore evident that HCC develops in a niche with mechanical properties

distinct from those encountered in the normal liver. Cancer development and progression is dependent on both intrinsic genetic abnormalities and external structural determinants.5 Matrix stiffness has recently been directly implicated in aiding tumor development. Increases in matrix stiffness that enhance cell contractility have been found to be sufficient to enhance the transformation of mammary epithelial cells.6 Conversely, a reduction in tissue stiffness by inhibition of collagen cross-linking impedes malignant growth and tumor development in a murine model of breast cancer.7 Cellular stiffness sensing relies upon intracellular tension, selleck compound which is determined by a dynamic equilibrium between forces generated by a contractile cytoskeleton

and the elastic resistance (stiffness) provided by the extracellular matrix (ECM). In this context, cancer progression (tumor growth, invasion, and dissemination) is accompanied by changes in both the mechanical properties of the cancer cell niche and changes in cellular contractility (modified by genetic and MCE epigenetic

factors) that regulate tumor cell behavior. HCC continues to have a poor prognosis (median survival less than 12 months), reflecting its late presentation and lack of effective therapies.8, 9 The effectiveness of both hepatic resection and liver transplantation for HCC is limited by tumor recurrence, which can occur months or years following resection of a primary tumor.10 Furthermore, systemic chemotherapy has proved ineffective both for the treatment of advanced HCC and in an adjuvant/neoadjuvant setting for the eradication of disseminated (dormant) tumor cells, the progenitors of clinical metastases. The mechanisms underlying chemotherapy resistance in HCC have not been fully elucidated. Although it has previously been demonstrated that the composition of the matrix can enhance chemotherapy resistance in a range of epithelial cancers,11, 12 the role of matrix stiffness has not been specifically addressed for HCC or other epithelial cancers. Here, we demonstrate that mechanical factors regulate both the proliferation and chemotherapeutic response of HCC cells. In addition, we show that both tumor cell differentiation and cancer stem cell characteristics are influenced by the mechanical properties (that is, stiffness) of the cancer cell niche.