Andreas Stylianou

Atomic Force Microscopy (AFM) nanoindentation is a powerful technique for determining the mechanical properties of soft samples at the nanoscale. The Hertz model is typically used for data processing when employing spherical indenters for small indentation depths (h) compared to the radius of the tip (R). When dealing with larger indentation depths, Sneddon’s equations can be used instead. In such cases, the fitting procedure becomes more intricate. Nevertheless, as the h/R ratio increases, the force–indentation curves tend to become linear. In this paper the potential of using the linear segment of the curve (for h > R) to determine Young’s modulus is explored. Force–indentation data from mouse and human lung tissues were utilized, and Young’s modulus was calculated using both conventional and linear approximation methods. The linear approximation proved to be accurate in all cases. Gaussian functions were applied to the results obtained from both classic Sneddon’s equations and the simplified approach, resulting in identical distribution means. Moreover, the simplified approach was notably unaffected by contact point determination. The linear segment of the force–indentation curve in deep spherical indentations can accurately determine the Young’s modulus of soft materials at the nanoscale.

As metastasis is responsible for most cancer-related deaths, understanding the cellular and molecular events that lead to cancer cell migration and invasion will certainly provide insights into novel anti-metastatic therapeutic targets. Fascin-1 is an actin-bundling protein fundamental to all physiological or pathological processes that require cell migration. It is responsible for cross-linking actin microfilaments during the formation of actin-rich cellular structures at the leading edge of migrating cells such as filopodia, lamellipodia and invadopodia. While most epithelial tissues express low levels of Fascin-1, it is dramatically elevated in the majority of cancers and its expression has been associated with more aggressive disease and decreased overall survival. Hence, it has been proposed as a potential anti-cancer target. In the present review, we studied recent literature with regard to Fascin-1 expression in different cancers, its role in altering the mechanical properties of cancer cells, promoting cancer cell migration, invasion and metastasis and the effect of its inhibition, via various pharmacological inhibitors, in eliminating metastasis in vitro and/or in vivo. Recent studies corroborate the notion that Fascin-1 is critically involved in metastasis and prove that it is a valuable anti-metastatic target that is worth investigating further.