Growth dysregulation and p53 accumulation in human primary colorectal cancer
1999

Growth Dysregulation and p53 in Colorectal Cancer

Sample size: 42 publication Evidence: moderate

Author Information

Author(s): Watson D S, Brotherick I, Shenton B K, Wilson R G, Campbell F C

Primary Institution: Department of Surgery, The Medical School, University of Newcastle

Hypothesis

The study investigates the relationship between p53 accumulation and growth homeostasis in colorectal cancer.

Conclusion

p53 accumulation in colorectal cancer is linked to reduced apoptosis, which may disrupt normal growth regulation.

Supporting Evidence

  • In normal mucosa, 10.3% of cells were in DNA synthesis phase while 28.7% showed apoptosis.
  • In cancers, 15.6% of cells were in DNA synthesis phase and 18.5% showed apoptosis.
  • p53 accumulation was detected in 59% of tumors and was associated with reduced apoptosis.

Takeaway

In colorectal cancer, a lot of cells are growing but not dying like they should, and this is related to a protein called p53.

Methodology

Flow cytometry was used to assess DNA content, cell cycle phases, and apoptosis in fresh colorectal tumors and matched normal mucosa, while p53 accumulation was evaluated through immunohistochemistry.

Statistical Information

P-Value

p<0.02

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1038/sj.bjc.6690464

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication