Mitomycin C induced chromosomal aberrations in young cancer patients. 1998

S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
Cell Biology Division, Division of Research, The Gujarat Cancer Society, The Gujarat Cancer and Research Institute, NCH Campus, Asarwa, Ahmedabad-380 016, India.gcri@adl.vsnl.net.in

Mitomycin-C (MMC) induced Chromosomal aberration (CA) frequencies were studied in 48 h peripheral blood lymphocyte (PBL) cultures of untreated cancer patients of young age (maximum age 12 years, n=77). Control population (n=71) consisted of age-matched group (maximum age 12 years, n=21); elder controls (minimum age 60 years, n=19) and healthy first degree relatives, i.e., parents or siblings of the pediatric cancer patients (mean age 24.3 years, n=31) as they share their genome and environment. Induced CA levels were found to be significantly higher among pediatric cancer patients as compared to control groups. The age-matched and elder control groups showed comparable CA levels. The first degree relatives controls showed higher induced CA levels as compared to pediatric and elder control groups. The present results indicate that there are different degrees of mutagen sensitivity prevailing in normal population. This may be responsible for differential cancer proneness. High degree of mutagen sensitivity in cancer patients may also be playing a major role in cancer onset at an early age.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009152 Mutagenicity Tests Tests of chemical substances and physical agents for mutagenic potential. They include microbial, insect, mammalian cell, and whole animal tests. Genetic Toxicity Tests,Genotoxicity Tests,Mutagen Screening,Tests, Genetic Toxicity,Toxicity Tests, Genetic,Genetic Toxicity Test,Genotoxicity Test,Mutagen Screenings,Mutagenicity Test,Screening, Mutagen,Screenings, Mutagen,Test, Genotoxicity,Tests, Genotoxicity,Toxicity Test, Genetic
D009369 Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. Benign Neoplasm,Cancer,Malignant Neoplasm,Tumor,Tumors,Benign Neoplasms,Malignancy,Malignant Neoplasms,Neoplasia,Neoplasm,Neoplasms, Benign,Cancers,Malignancies,Neoplasias,Neoplasm, Benign,Neoplasm, Malignant,Neoplasms, Malignant
D012044 Regression Analysis Procedures for finding the mathematical function which best describes the relationship between a dependent variable and one or more independent variables. In linear regression (see LINEAR MODELS) the relationship is constrained to be a straight line and LEAST-SQUARES ANALYSIS is used to determine the best fit. In logistic regression (see LOGISTIC MODELS) the dependent variable is qualitative rather than continuously variable and LIKELIHOOD FUNCTIONS are used to find the best relationship. In multiple regression, the dependent variable is considered to depend on more than a single independent variable. Regression Diagnostics,Statistical Regression,Analysis, Regression,Analyses, Regression,Diagnostics, Regression,Regression Analyses,Regression, Statistical,Regressions, Statistical,Statistical Regressions
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002675 Child, Preschool A child between the ages of 2 and 5. Children, Preschool,Preschool Child,Preschool Children
D002842 Chromatids Either of the two longitudinally adjacent threads formed when a eukaryotic chromosome replicates prior to mitosis. The chromatids are held together at the centromere. Sister chromatids are derived from the same chromosome. (Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed) Chromatid
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality

Related Publications

S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
August 1997, Yi chuan xue bao = Acta genetica Sinica,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
January 1978, Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abteilung: Mikrobiologie der Landwirtschaft der Technologie und des Umweltschutzes,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
April 1986, Mutation research,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
June 1976, Chromosoma,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
January 1983, Teratogenesis, carcinogenesis, and mutagenesis,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
April 2009, Mutation research,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
January 1989, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
January 2009, Medicinski pregled,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
July 1988, Mutation research,
S R Bakshi, and R K Patel, and S K Roy, and P Alladi, and A H Trivedi, and J M Bhatavdekar, and D D Patel, and P M Shah, and U M Rawal
January 1987, Neoplasma,
Copied contents to your clipboard!