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Biomedical subjects

S Kakati

Publications and source records attributed to S Kakati.

46 records · Page 3Linked to original sources
PubMed1975

Chromosomes and causation of human cancer and leukemia. X. Banding patterns in cancerous effusions.

Cells from five cancer effusions (two ovarian carcinomas, two lung cancers, and one carcinoma of the breast) were analyzed by G-, C-, and Q-banding techniques. The following observations were made: 1) The origin of some marker chromosomes could be traced accurately by these banding techniques. 2) Several chromosomes, which appeared normal with conventional staining techniques, were found to be re-arranged ones and, hence, abnormal. 3) Chromosomes No. 1, No. 3 and No. 11 were the most frequently involved in aberrations, whereas No. 12, No. 13, No. 17-20, and No. 22 Were least frequently involved. Only in one case each was the X chromosome or the Y chromosome involved in aberrations. The Y chromosome was found to be missing in all cancer cells of one lung cancer. 4) Each effusion had characteristic markers, invariably present in each cell, whether the cells were near diploid, or polyploid. 5) No common markers were observed in the two ovarian carcinomas studied, whereas the two lung cancers had a few common markers.

Adult↗
PubMedDate not supplied

Distribution and relation of radiation induced chromosomal aberrations in human lymphocytes as seen in the first and second cell cycles.

Different types of chromosomal damage in the G(o) phase of human lymphocytes have been studied in the first (M1) and second cell lymphocytes (M2). Large populations of cells containing one dicentric chromosome and one acentric (DIC+) were observed in the second cycle. This indicates that these dicentric and acentric fragments have a normal distribution in M2 or, arose through loss of one acentric fragment (AC) from cells containing one dicentric and two acentric fragments (DIC++) in M1. Similarly, a large number of metaphases in M2 have unpaired differentiated ACs. Our data indicates that aberrant metaphases containing single AC or a DIC+ may undergo normal cell division and that these cells may not represent cells in the first cycle only, as was suggested by earlier workers. For radiation experiments to G(o), a desirable time to harvest human lymphocyte cultures appears to be 72 hours and screening of M1 and M2 cells by sister chromatid differentiation.

Chromosome Aberrations↗
PubMedDate not supplied

The human int-1 gene is located at chromosome region 12q12-12q13 and is not rearranged in myxoid liposarcoma with t(12;16) (q13;p11).

The mouse cellular oncogene int-1 is often transcriptionally activated as a consequence of nearby proviral insertions in mouse mammary tumors. A highly conserved sequence has been found in the human genome, called int-1 gene, the role of which in human tumors is not known. By somatic hybrids, the human int-1 gene has been assigned to the segment 12q14-12pter. Using a genomic DNA clone containing the fourth exon of the human int-1 gene we have mapped the human int-1 gene to 12q12-12q13. To determine whether this gene, which is located close to the 12q13 breakpoint associated with myxoid liposarcoma, is rearranged in these tumors, we have performed Southern blot analysis of DNA from myxoid liposarcomas carrying the translocation t(12;16) (q13;p11). In the two tumors investigated, the translocation does not disrupt the int-1 gene.

Chromosome Mapping↗