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Related Concept Videos

Tumor Progression02:07

Tumor Progression

Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
Cancer02:18

Cancer

Cancers arise due to mutations in genes involved in the regulation of cell division, which leads to unrestricted cell proliferation. Modern science and medicine have made great strides in the understanding and treatment of cancer, including eradicating cancer in some patients. However, there is still no cure for cancer. This is largely due to the fact that cancer is a large group of many diseases.
Mutations01:35

Mutations

Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Mutations01:39

Mutations

Overview
Mutations01:39

Mutations

Overview
Cancer-Critical Genes I: Proto-oncogenes01:33

Cancer-Critical Genes I: Proto-oncogenes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...

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Related Experiment Video

Updated: May 11, 2026

Multi-Gene Single Nucleotide Polymorphism Detection in Gastric Cancer Based on Ion Semiconductor Sequencing Platform
06:21

Multi-Gene Single Nucleotide Polymorphism Detection in Gastric Cancer Based on Ion Semiconductor Sequencing Platform

Published on: May 10, 2024

Colorectal cancer: molecular mutations and polymorphisms.

Aga Syed Sameer1

  • 1Department of Biochemistry, Sher-I-Kashmir Institute of Medical Sciences Associated Medical College, Bemina, Srinagar Kashmir, India.

Frontiers in Oncology
|May 30, 2013
PubMed
Summary

Colorectal cancer (CRC) arises from chromosomal instability (CIN) or microsatellite instability (MIN) pathways. This review examines gene mutations and polymorphisms in these pathways crucial for CRC development.

Keywords:
colorectal cancerhypermethylationmedical geneticsmutationspolymorphism

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Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
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Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer

Published on: July 28, 2010

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Multi-Gene Single Nucleotide Polymorphism Detection in Gastric Cancer Based on Ion Semiconductor Sequencing Platform
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Published on: May 10, 2024

Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
28:15

Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer

Published on: July 28, 2010

Area of Science:

  • Oncology
  • Genetics
  • Cancer Biology

Background:

  • Colorectal cancer (CRC) is a leading cause of cancer-related death globally, ranking third in men and second in women.
  • CRC incidence varies significantly across different racial and ethnic populations.
  • Tumorigenesis in CRC involves chromosomal instability (CIN), microsatellite instability (MIN), genetic mutations, and epigenetic alterations.

Purpose of the Study:

  • To review mutations and polymorphisms in key genes within the CIN and MIN pathways.
  • To highlight genetic factors contributing to colorectal cancer development.

Main Methods:

  • Literature review focusing on genetic mutations and polymorphisms.
  • Analysis of genes involved in chromosomal instability (CIN) and microsatellite instability (MIN) pathways.

Main Results:

  • Identified critical gene mutations and polymorphisms in CIN and MIN pathways implicated in CRC.
  • Detailed the genetic underpinnings of CRC development through these instability pathways.

Conclusions:

  • Gene mutations and polymorphisms in CIN and MIN pathways are fundamental to colorectal cancer development.
  • Understanding these genetic alterations is vital for future CRC research and therapeutic strategies.