9 research outputs found
Cancer recurrence times from a branching process model
As cancer advances, cells often spread from the primary tumor to other parts
of the body and form metastases. This is the main cause of cancer related
mortality. Here we investigate a conceptually simple model of metastasis
formation where metastatic lesions are initiated at a rate which depends on the
size of the primary tumor. The evolution of each metastasis is described as an
independent branching process. We assume that the primary tumor is resected at
a given size and study the earliest time at which any metastasis reaches a
minimal detectable size. The parameters of our model are estimated
independently for breast, colorectal, headneck, lung and prostate cancers. We
use these estimates to compare predictions from our model with values reported
in clinical literature. For some cancer types, we find a remarkably wide range
of resection sizes such that metastases are very likely to be present, but none
of them are detectable. Our model predicts that only very early resections can
prevent recurrence, and that small delays in the time of surgery can
significantly increase the recurrence probability.Comment: 26 pages, 9 figures, 4 table
A community-sourced glossary of open scholarship terms
Supplementary Information: This list of terms represents the ‘Open Scholarship Glossary 1.0’ (available at: https://forrt.org/glossary/. Glossary available under a CC BY NC SA 4.0 license at: https://static-content.springer.com/esm/art%3A10.1038%2Fs41562-021-01269-4/MediaObjects/41562_2021_1269_MOESM1_ESM.pdf).https://static-content.springer.com/esm/art%3A10.1038%2Fs41562-021-01269-4/MediaObjects/41562_2021_1269_MOESM1_ESM.pd
A community-sourced glossary of open scholarship terms
Open scholarship has transformed research, introducing a host of new terms in the lexicon of researchers. The Framework of Open and Reproducible Research Teaching (FORRT) community presents a crowd-sourced glossary of open scholarship terms to facilitate education and effective communication between experts and newcomers
Development of a Cell-penetrating Peptide that Exhibits Responsive Changes in its Secondary Structure in the Cellular Environment
Thermohydrodynamic (THD) Analysis of Journal Bearing Operating with Bio-based Nanolubricants
Solid State Polymorphism of Isotactic and Syndiotactic Polypropylene
The crystal structure and polymorphism of isotactic (iPP) and syndioactic polypropylene (sPP) are illustrated, highlighting the rich variety of phase behavior of these polymers, the conditions of obtainment of the different polymorphs and the disorder phenomena occurring in the crystals. After description of the concepts of packing and conformational polymorphism occurring in the case of iPP and sPP respectively, the crystal structure of the different polymorphs of iPP and sPP are described. In particular, the main structural features relative to the monoclinc α-, the trigonal β- and the orthorhombic γ-forms, of iPP including the mesomorphic form, and the trigonal form which develops in random isotactic copolymers of propylene with pentene or hexene units, are described at first, the chain conformation in all these polymorphs being the 3/1 helix. Then, the complex polymorphism of sPP and the crystal structure of the orthorhombic helical form I and II, the orthorhombic trans-planar form III, the monoclininc form IV, and the trans-planar and helical mesophases are illustrated. The implications of the crystal structure with the final properties are outlined for these polymers, the great fortune of which was the almost simultaneous discovery of the polymerization catalyst systems and the structural elucidation