Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Ras protein abundance correlates with Ras isoform mutation patterns in cancer
by
Jenkins, Rosalind E.
, Sahraoui, Yasmina M.
, Hood, Fiona E.
, Prior, Ian A.
in
631/67/395
/ 631/67/70
/ 631/80/86
/ 82
/ 82/58
/ Apoptosis
/ Cancer
/ Cell Biology
/ Codons
/ Dosage
/ Gene duplication
/ HRAS protein
/ Human Genetics
/ Humans
/ Internal Medicine
/ Isoforms
/ K-Ras protein
/ Medicine
/ Medicine & Public Health
/ Mutants
/ Mutation
/ Neoplasms - genetics
/ Neoplasms - metabolism
/ Oncology
/ Protein Isoforms - genetics
/ Protein Isoforms - metabolism
/ Proteins
/ Proto-Oncogene Proteins p21(ras) - genetics
/ Proto-Oncogene Proteins p21(ras) - metabolism
/ Ras protein
/ ras Proteins - genetics
/ ras Proteins - metabolism
/ Signal Transduction
/ Tumorigenesis
2023
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Ras protein abundance correlates with Ras isoform mutation patterns in cancer
by
Jenkins, Rosalind E.
, Sahraoui, Yasmina M.
, Hood, Fiona E.
, Prior, Ian A.
in
631/67/395
/ 631/67/70
/ 631/80/86
/ 82
/ 82/58
/ Apoptosis
/ Cancer
/ Cell Biology
/ Codons
/ Dosage
/ Gene duplication
/ HRAS protein
/ Human Genetics
/ Humans
/ Internal Medicine
/ Isoforms
/ K-Ras protein
/ Medicine
/ Medicine & Public Health
/ Mutants
/ Mutation
/ Neoplasms - genetics
/ Neoplasms - metabolism
/ Oncology
/ Protein Isoforms - genetics
/ Protein Isoforms - metabolism
/ Proteins
/ Proto-Oncogene Proteins p21(ras) - genetics
/ Proto-Oncogene Proteins p21(ras) - metabolism
/ Ras protein
/ ras Proteins - genetics
/ ras Proteins - metabolism
/ Signal Transduction
/ Tumorigenesis
2023
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Ras protein abundance correlates with Ras isoform mutation patterns in cancer
by
Jenkins, Rosalind E.
, Sahraoui, Yasmina M.
, Hood, Fiona E.
, Prior, Ian A.
in
631/67/395
/ 631/67/70
/ 631/80/86
/ 82
/ 82/58
/ Apoptosis
/ Cancer
/ Cell Biology
/ Codons
/ Dosage
/ Gene duplication
/ HRAS protein
/ Human Genetics
/ Humans
/ Internal Medicine
/ Isoforms
/ K-Ras protein
/ Medicine
/ Medicine & Public Health
/ Mutants
/ Mutation
/ Neoplasms - genetics
/ Neoplasms - metabolism
/ Oncology
/ Protein Isoforms - genetics
/ Protein Isoforms - metabolism
/ Proteins
/ Proto-Oncogene Proteins p21(ras) - genetics
/ Proto-Oncogene Proteins p21(ras) - metabolism
/ Ras protein
/ ras Proteins - genetics
/ ras Proteins - metabolism
/ Signal Transduction
/ Tumorigenesis
2023
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Ras protein abundance correlates with Ras isoform mutation patterns in cancer
Journal Article
Ras protein abundance correlates with Ras isoform mutation patterns in cancer
2023
Request Book From Autostore
and Choose the Collection Method
Overview
Activating mutations of Ras genes are often observed in cancer. The protein products of the three Ras genes are almost identical. However, for reasons that remain unclear, KRAS is far more frequently mutated than the other Ras isoforms in cancer and RASopathies. We have quantified HRAS, NRAS, KRAS4A and KRAS4B protein abundance across a large panel of cell lines and healthy tissues. We observe consistent patterns of KRAS > NRAS»HRAS protein expression in cells that correlate with the rank order of Ras mutation frequencies in cancer. Our data provide support for the model of a sweet-spot of Ras dosage mediating isoform-specific contributions to cancer and development. We suggest that in most cases, being the most abundant Ras isoform correlates with occupying the sweet-spot and that HRAS and NRAS expression is usually insufficient to promote oncogenesis when mutated. However, our results challenge the notion that rare codons mechanistically underpin the predominance of KRAS mutant cancers. Finally, direct measurement of mutant versus wildtype KRAS protein abundance revealed a frequent imbalance that may suggest additional non-gene duplication mechanisms for optimizing oncogenic Ras dosage.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
This website uses cookies to ensure you get the best experience on our website.