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Related Concept Videos

The Ras Gene02:38

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The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
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Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
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Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
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Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
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Characterize Disease-related Mutants of RAF Family Kinases by Using a Set of Practical and Feasible Methods
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The Frequency of Ras Mutations in Cancer.

Ian A Prior1, Fiona E Hood2, James L Hartley3

  • 1Division of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom. iprior@liv.ac.uk.

Cancer Research
|March 27, 2020
PubMed
Summary
This summary is machine-generated.

Approximately 19% of cancer patients have Ras mutations, equating to 3.4 million new cases annually worldwide. This study clarifies Ras mutation frequency across all cancer types and isoforms for targeted therapy insights.

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Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Ras proteins are frequently mutated in various cancers.
  • Existing literature shows significant variability (10%-30%) in reported Ras mutation frequencies.
  • This inconsistency stems from data aggregation biases and the influence of specific cancer types and Ras isoforms.

Purpose of the Study:

  • To establish a definitive Ras mutation frequency across all major cancer types and isoforms.
  • To estimate the global annual incidence of Ras-mutant cancers.
  • To identify Ras isoform and mutation-specific trends relevant for targeted therapies.

Main Methods:

  • Cross-referencing data from all major publicly accessible cancer mutation databases.
  • Calculating reliable mutation frequency values for each Ras isoform in all major cancer types.
  • Applying these frequencies to U.S. cancer incidence statistics for global estimations.

Main Results:

  • Approximately 19% of all cancer patients harbor Ras mutations.
  • This equates to an estimated 3.4 million new Ras-mutant cancer cases worldwide annually.
  • Significant trends in Ras isoform and mutation prevalence across different cancer types were identified.

Conclusions:

  • Ras mutations are present in approximately 19% of cancer patients globally.
  • The findings provide a more accurate estimate of Ras mutation burden in cancer.
  • Understanding these mutation patterns is crucial for developing and refining Ras-targeted cancer therapies.