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Pregled bibliografske jedinice broj: 2226

Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas


Krušlin, Božidar; Hrašćan, Reno; Manojlović, Spomenka; Pavelić, Krešimir
Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas // Pediatric pathology & laboratory medicine, 17 (1997), 1; 43-52 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 2226 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas

Autori
Krušlin, Božidar ; Hrašćan, Reno ; Manojlović, Spomenka ; Pavelić, Krešimir

Izvornik
Pediatric pathology & laboratory medicine (1077-1042) 17 (1997), 1; 43-52

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
oncogenes; p53; ras; sacrococcygeal teratoma; tumor suppressor genes

Sažetak
Congenital sacrococcygeal teratoma (SCT) is the most common germ cell tumor of infancy and childhood with a female preponderance. Most SCTs are diagnosed at birth, are benign, and consist of fully differentiated, mature tissues. Tumorigenesis of SCTs remains poorly understood. Almost nothing is known about possible oncogene activation or tumor suppressor inactivation in these rare tuners. We describe the presence of various oncoproteins and tumor suppressor proteins in eight cases of congenital SCT. The following oncogenes were examined: ras family (c-H-, c-N-, and c-K-ras), early genes (fos, jun), and tumor suppressor genes (p53 and nm23-H-1). There was no relationship between the intensity of expression of these oncoproteins and tumor suppressor genes and the following parameters: tumor size, age, and survival of the patients. We did not observe any difference, however, between the expression of the examined oncogenes and tumor suppressor genes nm23 and p53 in immature and mature teratomas. Our findings suggest that the ras family of oncogenes, fos and jun oncogenes, and nm23 and p53 tumor suppressor genes are present in congenital SCT, indicating a possible role in genesis and development of these tumors. [References: 23]

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
00981104
101751

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Hrvatska akademija znanosti i umjetnosti


Citiraj ovu publikaciju:

Krušlin, Božidar; Hrašćan, Reno; Manojlović, Spomenka; Pavelić, Krešimir
Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas // Pediatric pathology & laboratory medicine, 17 (1997), 1; 43-52 (međunarodna recenzija, članak, znanstveni)
Krušlin, B., Hrašćan, R., Manojlović, S. & Pavelić, K. (1997) Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas. Pediatric pathology & laboratory medicine, 17 (1), 43-52.
@article{article, author = {Kru\v{s}lin, Bo\v{z}idar and Hra\v{s}\'{c}an, Reno and Manojlovi\'{c}, Spomenka and Paveli\'{c}, Kre\v{s}imir}, year = {1997}, pages = {43-52}, keywords = {oncogenes, p53, ras, sacrococcygeal teratoma, tumor suppressor genes}, journal = {Pediatric pathology and laboratory medicine}, volume = {17}, number = {1}, issn = {1077-1042}, title = {Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas}, keyword = {oncogenes, p53, ras, sacrococcygeal teratoma, tumor suppressor genes} }
@article{article, author = {Kru\v{s}lin, Bo\v{z}idar and Hra\v{s}\'{c}an, Reno and Manojlovi\'{c}, Spomenka and Paveli\'{c}, Kre\v{s}imir}, year = {1997}, pages = {43-52}, keywords = {oncogenes, p53, ras, sacrococcygeal teratoma, tumor suppressor genes}, journal = {Pediatric pathology and laboratory medicine}, volume = {17}, number = {1}, issn = {1077-1042}, title = {Oncoproteins and tumor suppressor proteins in congenital sacrococcygeal teratomas}, keyword = {oncogenes, p53, ras, sacrococcygeal teratoma, tumor suppressor genes} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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