Ur Rehman, A. | bioRxiv Science

bioRxiv2023

Mode III tear resistance of Bombyx mori silk cocoons

This paper concerns the tear properties and behaviour of Bombyx mori silk cocoons. The tear resistance of cocoon layers is found to increase progressively from the innermost layer to the outermost layer. Importantly, the increase in tear strength correlates with increased porosity, which itself affects fibre mobility. We propose a microstructural mechanism for tear failure, which begins with fibre stretching and sliding, leading to fibre piling, and eventuating in fibre fracture. The direction of fracture is then deemed to be a function of the orientation of piled fibres, which is influenced by the presence of junctions where fibres cross at different angles and which may then acts as nucleating sites for fibre piling. The interfaces between cocoon wall layers in Bombyx mori cocoon walls account for 38% of the total wall tear strength. When comparing the tear energies and densities of Bombyx mori cocoon walls against other materials, we find that the Bombyx mori cocoon walls exhibit a balanced trade-off between tear resistance and lightweightness.

zoology↗

bioRxiv2020

CBX2 and CBX7 antagonistically regulate metabolic reprogramming in breast cancer

Striking similarity exists between metabolic changes associated with embryogenesis and tumorigenesis. Chromobox proteins-CBX2/4/6/7/8, core components of canonical polycomb repressor complex 1 (cPRC1), play essential roles in embryonic development and aberrantly expressed in breast cancer. Understanding how altered CBX expression relates to metabolic reprogramming in breast cancer may reveal vulnerabilities of therapeutic pertinence. Using transcriptomic and metabolomic data from breast cancer patients (N>3000 combined), we performed pathway-based analysis and identified outstanding roles of CBX2 and CBX7 in positive and negative regulation of glucose metabolism, respectively. Genetic ablation experiments validated the contrasting roles of two isoforms in cancer metabolism and cell growth. Furthermore, we provide evidence for the role of mTORC1 signaling in mediating contrary effects of CBX2 and CBX7 on breast cancer metabolism. Underpinning the biological significance of metabolic roles, CBX2 and CBX7 were found to be the most up- and down-regulated isoforms, respectively, in breast tumors compared to normal tissues. Moreover, CBX2 and CBX7 expression (not other isoforms) correlated strongly, but oppositely, with breast tumor subtype aggressiveness and the proliferation markers. Consistently, genomic data also showed higher amplification frequency of CBX2, not CBX7, in breast tumors. Highlighting the clinical significance of findings, disease-specific survival and drug sensitivity analysis revealed that CBX2 and CBX7 predicted patient outcome and sensitivity to FDA-approved clinical drugs. In summary, this work identifies novel cross-talk between CBX2/7 and breast tumor metabolism, and the results presented may have implications in strategies targeting breast cancer.

cancer biology↗