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Clonal divergence in lung cancer development is associated with allelic loss on chromosome 4
Author(s) -
Banerjee A. K.,
Read C. A.,
Griffiths M. H.,
George P. J.,
Rabbitts P. H.
Publication year - 2007
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/gcc.20472
Subject(s) - loss of heterozygosity , biology , metastasis , primary tumor , lung cancer , carcinogenesis , cancer research , malignancy , tumor suppressor gene , cancer , pathology , allele , gene , genetics , medicine
Patients who receive curative treatment for lung cancer can develop additional lung tumors that may or may not be related to the original tumor and thus require different clinical management. If a subsequent tumor has a pattern of allele loss, revealed by allelotype analysis, overlapping that of the first tumor, it is believed to be a local recurrence or metastasis. In this case history, we present loss of heterozygosity analyses of the original primary tumor, and two second primary tumors occurring in the ipsilateral and the contra‐lateral lungs. The allelotyping suggests that these tumors are all clonally related but concordance is not complete. Our interpretation is that the original primary tumor and the two new primary tumors have developed to full malignancy independently, but are clonally related, possibly via a clone of motile progenitor cells. Deletion mapping of DNA from biopsies of this patient delineated a region in 4p16 that we had previously shown to be lost in the transition from carcinoma in situ to invasive tumor. We identified a minimally deleted region encompassing six genes including two candidate tumor supprressor genes, CRMP1 a lung cancer metastasis‐suppressing gene and PPP2R2C a gene for a regulatory subunit of the PP2 complex known to suppress tumorigenesis, particularly viral induced transformation. © 2007 Wiley‐Liss, Inc.