collection
https://read.qxmd.com/read/34516744/tumor-draining-lymph-nodes-at-the-crossroads-of-metastasis-and-immunity
#1
JOURNAL ARTICLE
Haley du Bois, Taylor A Heim, Amanda W Lund
[Figure: see text].
September 10, 2021: Science Immunology
https://read.qxmd.com/read/32433532/a-guide-to-cancer-immunotherapy-from-t-cell-basic-science-to-clinical-practice
#2
REVIEW
Alex D Waldman, Jill M Fritz, Michael J Lenardo
The T lymphocyte, especially its capacity for antigen-directed cytotoxicity, has become a central focus for engaging the immune system in the fight against cancer. Basic science discoveries elucidating the molecular and cellular biology of the T cell have led to new strategies in this fight, including checkpoint blockade, adoptive cellular therapy and cancer vaccinology. This area of immunological research has been highly active for the past 50 years and is now enjoying unprecedented bench-to-bedside clinical success...
November 2020: Nature Reviews. Immunology
https://read.qxmd.com/read/33911231/the-inflammatory-pathogenesis-of-colorectal-cancer
#3
REVIEW
Mark Schmitt, Florian R Greten
The mutational landscape of colorectal cancer (CRC) does not enable predictions to be made about the survival of patients or their response to therapy. Instead, studying the polarization and activation profiles of immune cells and stromal cells in the tumour microenvironment has been shown to be more informative, thus making CRC a prototypical example of the importance of an inflammatory microenvironment for tumorigenesis. Here, we review our current understanding of how colon cancer cells interact with their microenvironment, comprised of immune cells, stromal cells and the intestinal microbiome, to suppress or escape immune responses and how inflammatory processes shape the immune pathogenesis of CRC...
October 2021: Nature Reviews. Immunology
https://read.qxmd.com/read/34433962/the-mutational-landscape-of-human-somatic-and-germline-cells
#4
JOURNAL ARTICLE
Luiza Moore, Alex Cagan, Tim H H Coorens, Matthew D C Neville, Rashesh Sanghvi, Mathijs A Sanders, Thomas R W Oliver, Daniel Leongamornlert, Peter Ellis, Ayesha Noorani, Thomas J Mitchell, Timothy M Butler, Yvette Hooks, Anne Y Warren, Mette Jorgensen, Kevin J Dawson, Andrew Menzies, Laura O'Neill, Calli Latimer, Mabel Teng, Ruben van Boxtel, Christine A Iacobuzio-Donahue, Inigo Martincorena, Rakesh Heer, Peter J Campbell, Rebecca C Fitzgerald, Michael R Stratton, Raheleh Rahbari
Over the course of an individual's lifetime, normal human cells accumulate mutations1 . Here we compare the mutational landscape in 29 cell types from the soma and germline using multiple samples from the same individuals. Two ubiquitous mutational signatures, SBS1 and SBS5/40, accounted for the majority of acquired mutations in most cell types, but their absolute and relative contributions varied substantially. SBS18, which potentially reflects oxidative damage2 , and several additional signatures attributed to exogenous and endogenous exposures contributed mutations to subsets of cell types...
September 2021: Nature
https://read.qxmd.com/read/26404825/somatic-mutation-in-cancer-and-normal-cells
#5
REVIEW
IƱigo Martincorena, Peter J Campbell
Spontaneously occurring mutations accumulate in somatic cells throughout a person's lifetime. The majority of these mutations do not have a noticeable effect, but some can alter key cellular functions. Early somatic mutations can cause developmental disorders, whereas the progressive accumulation of mutations throughout life can lead to cancer and contribute to aging. Genome sequencing has revolutionized our understanding of somatic mutation in cancer, providing a detailed view of the mutational processes and genes that drive cancer...
September 25, 2015: Science
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