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Updated: Jul 19, 2026

Comparative Lesions Analysis Through a Targeted Sequencing Approach
Published on: November 5, 2019
Chromosome 18q deletion and Smad4 protein inactivation correlate with liver metastasis: A study matched for T- and N-
T Tanaka1, T Watanabe, Y Kazama
1Department of Surgical Oncology, University of Tokyo, 7-3-1 Hongo, Bunkyo-Ku, Tokyo, Japan.
Abstract:
Smad4 protein, whose gene is coded at chromosome 18q21.1, is an important tumour suppressor that mediates transforming growth factor-beta. It has been reported that inactivation of the Smad4 gene and allelic loss of chromosome 18q correlate with liver metastasis and poorer prognosis in colorectal cancers. Utilising a recently developed method of immunohistochemical staining for Smad4 protein, we focused on the specific impact of Smad4 protein expression on liver metastasis in colorectal cancer. We also evaluated the association between chromosome18q deletion and liver metastasis. We selected 20 colorectal cancers with liver metastasis for the experimental group, and 20 cases without liver metastasis for the control. In order to exclude the influence of lymph node metastasis, all cases were lymph node negative. In addition, the two groups were matched for tumour depth, tumour differentiation and tumour location. We compared the expression level of Smad4 protein immunohistochemically in these 20 matched pairs. We also compared the loss of heterozygosity status at chromosome 18q in these 20 matched pairs. Immunohistochemical staining revealed a significant difference (P = 0.024) in the level of Smad4 protein between the two groups. We also observed a significantly different (P=0.0054) ratio of allelic deletion at chromosome 18q21. Smad4 protein expression level and allelic loss at 18q21 are associated with the process of liver metastasis in colorectal cancers evaluated when excluding clinical and pathological features except for liver metastasis.
Insights
Smad4 protein loss and chromosome 18q deletion are linked to liver metastasis in colorectal cancer. This suggests their potential as biomarkers for predicting cancer spread and patient prognosis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Smad4 protein, a tumor suppressor, is crucial for transforming growth factor-beta signaling.
- Inactivation of the Smad4 gene and 18q chromosomal loss are associated with liver metastasis and poor prognosis in colorectal cancers.
Purpose of the Study:
- To investigate the specific impact of Smad4 protein expression on liver metastasis in colorectal cancer.
- To evaluate the association between chromosome 18q deletion and liver metastasis in colorectal cancer.
Main Methods:
- Utilized immunohistochemical staining to assess Smad4 protein expression.
- Analyzed loss of heterozygosity at chromosome 18q.
- Compared 20 lymph node-negative colorectal cancer cases with liver metastasis against 20 matched cases without metastasis.
Main Results:
- A significant difference in Smad4 protein expression was observed between groups (P = 0.024).
- A significantly different ratio of allelic deletion at chromosome 18q21 was found (P = 0.0054).
- Smad4 protein expression and 18q21 allelic loss are associated with liver metastasis in colorectal cancer.
Conclusions:
- Smad4 protein expression levels and 18q21 allelic status are significantly associated with liver metastasis in colorectal cancer.
- These factors may serve as potential biomarkers for predicting liver metastasis and prognosis in colorectal cancer patients.
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