Literature DB >> 6948415

Decreased tumorigenicity of rodent cells after fusion with leukocytes from normal and leukemic donors.

A H Geurts van Kessel, W C den Boer, A J van Agthoven, A Hagemeijer.   

Abstract

Interspecific hybrid cells, derived from fusion of normal and leukemic (CML) human leukocytes with tumorigenic P19 mouse or a3 Chinese hamster cells, were tested for their tumor-forming capacity in congenitally athymic nude mice. Partial suppression of tumorigenicity was observed in several hybrid clones derived from both normal and leukemic leukocytes. Chromosome analysis of the hybrid cells before inoculation in nude mice and of the derived tumors did not reveal a human chromosome bearing factor(s) which singly appeared responsible for suppression. The presence of the Philadelphia translocation in the leukemic cells does not seem to have deprived these cells of their tumor-suppressing ability.

Entities:  

Mesh:

Year:  1981        PMID: 6948415     DOI: 10.1007/bf01538754

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  11 in total

1.  Identification and characterization of satellite III subfamilies to the acrocentric chromosomes.

Authors:  R Bandyopadhyay; C McQuillan; S L Page; K H Choo; L G Shaffer
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

2.  A homologous subfamily of satellite III DNA on human chromosomes 14 and 22.

Authors:  K H Choo; E Earle; C McQuillan
Journal:  Nucleic Acids Res       Date:  1990-10-11       Impact factor: 16.971

3.  Four distinct alpha satellite subfamilies shared by human chromosomes 13, 14 and 21.

Authors:  B Vissel; K H Choo
Journal:  Nucleic Acids Res       Date:  1991-01-25       Impact factor: 16.971

4.  A chromosome 14-specific human satellite III DNA subfamily that shows variable presence on different chromosomes 14.

Authors:  K H Choo; E Earle; B Vissel; P Kalitsis
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

5.  Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter.

Authors:  J P Dumanski; A H Geurts van Kessel; M Ruttledge; A Wladis; N Sugawa; V P Collins; M Nordenskjöld
Journal:  Hum Genet       Date:  1990-02       Impact factor: 4.132

6.  Regional mapping of two human immunoglobulin V lambda genes and analysis of the V lambda locus in chronic myeloid leukaemia.

Authors:  M L Anderson; M H Goyns; A M Geurts van Kessel; B D Young
Journal:  Nucleic Acids Res       Date:  1985-08-26       Impact factor: 16.971

7.  Identification of a single chromosome in the normal human genome essential for suppression of hamster cell transformation.

Authors:  A Stoler; N Bouck
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

8.  Human lens gamma-crystallin sequences are located in the p12-qter region of chromosome 2.

Authors:  J T den Dunnen; R J Jongbloed; A H Geurts van Kessel; J G Schoenmakers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome.

Authors:  H Kurahashi; K Akagi; K Karakawa; T Nakamura; J P Dumanski; T Sano; S Okada; S Takai; I Nishisho
Journal:  Hum Genet       Date:  1994-03       Impact factor: 4.132

10.  The human homologue of the mouse t-complex gene, TCP1, is located on chromosome 6 but is not near the HLA region.

Authors:  K Willison; A Kelly; K Dudley; P Goodfellow; N Spurr; V Groves; P Gorman; D Sheer; J Trowsdale
Journal:  EMBO J       Date:  1987-07       Impact factor: 11.598

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