The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.
Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma
Abstract
In an allelotyping study of prostatic carcinoma, we found the highest frequency of allelic deletions on chromosomes 8, 10, 16, and 18. In all cases with allelic deletions, at least one of the chromosomes 8, 10, and 16 were involved. A detailed deletion mapping of these chromosomes in 18 cases was carried out with probes that detect restriction fragment length polymorphisms (RFLP) on chromosomes 8 (6 probes), 10(11 probes), and 16 (9 probes). The highest frequency of allelic deletions were found on 8p (65%), where the minimally deleted region was between the PLA T locus and pter. The long arm of chromosome 16 had allelic deletions in 56% of informative cases, with three different break points, the most distal being located between D16S4 and D16S7. Chromosome 10 exhibited a complex deletion pattern with terminal deletions of the p or the q arm (2 cases each), a deletion pattern that could be interpreted as nonreciprocal translocations of the q arm (2 cases), or allelic losses on all informative loci, suggesting monosomy (2 cases). Our data suggest that tumor suppressor genes involved in the oncogenesis of prostatic carcinoma may be localized between 8 pter and the PLAT locus and that additional/alternative tumor suppressor genes may be localized on chromosome 10 and on the long arm of chromosome 16 distal to the D16S4 locus.
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Roles for Nkx3.1 in prostate development and cancer
Bhatia-Gaur, R., Donjacour, A. A., Sciavolino, P. J., Kim, M., Desai, N., Young, P., Norton, C. R., Gridley, T., Cardiff, R. D., Cunha, G. R., et al. (1999) · Genes & Development · doi:10.1101/gad.13.8.966 · Cited by 665
Mutations of the human E-cadherin (CDH1) gene
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LNCaP progression model of human prostate cancer: Androgen-independence and osseous metastasis
Thalmann, G. N., Sikes, R. A., Wu, T. T., Degeorges, A., Chang, S.-M., Ozen, M., Pathak, S., & Chung, L. W. K. (2000) · The Prostate · doi:10.1002/1097-0045(20000701)44:2<91::aid-pros1>3.0.co;2-l · Cited by 366
Zhang, M., Magit, D., & Sager, R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.11.5673 · Cited by 158
Characterization of chromosomal abnormalities in prostate cancer cell lines by spectral karyotyping
Pan, Y., Kytölä, S., Farnebo, F., Wang, N., Lui, W. O., Nupponen, N., Isola, J., Visakorpi, T., Bergerheim, U. S. R., & Larsson, C. (1999) · Cytogenetic and Genome Research · doi:10.1159/000015432 · Cited by 63
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Metadata
- Authors
- Bergerheim, U. S. R., Kunimi, K., Collins, V. P., & Ekman, P.
- Venue
- Genes, Chromosomes and Cancer
- Publisher
- Wiley
- Published
- 1991-05
- Volume
- 3
- Issue
- 3
- Pages
- 215-220
- ISSN
- 1045-2257 (ISSN-L)
- 1098-2264
- OpenAlex
- W2012924225
- Cited by
- 290
- References
- 10
- FWCI
- 23.73
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma. https://app.cochat.ai/papers/10.1002/gcc.2870030308
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- Bergerheim, U. S. R., Kunimi, K., Collins, V. P., & Ekman, P. (1991). Deletion mapping of chromosomes 8, 10, and 16 in human prostatic carcinoma. Genes, Chromosomes and Cancer. https://doi.org/10.1002/gcc.2870030308
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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