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DCC tumor suppressor gene is inactivated in hematologic malignancies showing monosomy 18
E Porfiri1, L M Secker-Walker, A V Hoffbrand
1Department of Haematology, Royal Free Hospital School of Medicine, London, UK.
Abstract:
DCC (deleted in colorectal cancer) is a candidate tumor suppressor gene recently identified on chromosome band 18q21. Loss of one DCC allele or decreased DCC expression occurs in more than 70% of colorectal cancers, suggesting that DCC inactivation constitutes a critical event in the development of these tumors. Using polymerase chain reaction amplification of cDNA, we have studied DCC expression in bone marrow from 4 patients with leukemia (1 chronic myeloid leukemia-blastic crisis, case 1; 1 acute myeloid leukemia, case 2; 1 T-cell acute lymphoblastic leukemia [ALL], case 3; 1 B-cell ALL, case 4) showing loss of one DCC allele due to monosomy 18. We also studied DCC expression in multiple control samples, including normal lymphocytes, normal tonsillar tissue, and leukemias without 18q abnormalities. Four primer pairs consistently amplified the predicted DCC sequences from cDNA prepared from all control samples. However, in samples with monosomy 18, DCC transcripts were either not detected (case 1) or detected at a very low level (cases 2, 3, and 4). Southern analysis showed no structural rearrangement of the remaining DCC locus in all leukemia samples. Thus, loss of DCC expression was demonstrated in association with loss of one DCC allele in all cases tested. These results suggest that, as for colorectal tumors, the inactivation of DCC can have a role in the development of hematologic malignancies.
Insights
The deleted in colorectal cancer (DCC) gene, a tumor suppressor, showed reduced expression in leukemia patients with a lost DCC allele. This suggests DCC inactivation may contribute to blood cancer development.
Area of Science:
- Oncology
- Genetics
- Hematology
Background:
- The deleted in colorectal cancer (DCC) gene is a candidate tumor suppressor located at 18q21.
- Loss of DCC alleles or decreased expression is observed in over 70% of colorectal cancers.
- DCC inactivation is considered a critical event in colorectal tumor development.
Purpose of the Study:
- To investigate DCC gene expression in leukemia patients with monosomy 18.
- To determine if DCC inactivation plays a role in hematologic malignancies.
Main Methods:
- Studied DCC expression in bone marrow from four leukemia patients with monosomy 18 using polymerase chain reaction amplification of cDNA.
- Analyzed DCC expression in control samples including normal lymphocytes, tonsillar tissue, and leukemias without 18q abnormalities.
- Performed Southern analysis to detect structural rearrangements of the DCC locus.
Main Results:
- DCC transcripts were undetectable or very low in leukemia samples with monosomy 18.
- Control samples showed consistent amplification of DCC sequences.
- No structural rearrangements of the DCC locus were found in the leukemia samples.
Conclusions:
- Loss of DCC expression is associated with the loss of one DCC allele in the tested leukemia cases.
- DCC inactivation may play a role in the development of hematologic malignancies, similar to its role in colorectal tumors.