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Pregled bibliografske jedinice broj: 728990

Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin


Kafka, Anja; Tomas, Davor; Beroš, Vili; Pećina, Hrvoje Ivan; Zeljko, Martina; Pećina-Šlaus, Nives
Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin // International journal of molecular sciences, 15 (2014), 6; 10635-10651 doi:10.3390/ijms150610635 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 728990 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin

Autori
Kafka, Anja ; Tomas, Davor ; Beroš, Vili ; Pećina, Hrvoje Ivan ; Zeljko, Martina ; Pećina-Šlaus, Nives

Izvornik
International journal of molecular sciences (1422-0067) 15 (2014), 6; 10635-10651

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

Ključne riječi
Dishevelled-1 (DVL1); Dishevelled-3 (DVL3); E-cadherin (CDH1); beta-catenin (CTNNB1); brain metastases; lung cancer; immunostaining; loss of heterozygosity

Sažetak
The susceptibility of brain to secondary formation from lung cancer primaries is a well-known phenomenon. In contrast, the molecular basis for invasion and metastasis to the brain is largely unknown. In the present study, 31 brain metastases that originated from primary lung carcinomas were analyzed regarding over expression of Dishevelled-1 (DVL1), Dishevelled-3 (DVL3), E-cadherin (CDH1) and beta-catenin (CTNNB1). Protein expressions and localizations were analyzed by immunohistochemistry. Genetic alterations of E-cadherin were tested by polymerase chain reaction (PCR)/loss of heterozygosity (LOH). Heteroduplex was used to investigate mutations in beta-catenin. DVL1 and DVL3 showed over expression in brain metastasis in 87.1% and 90.3% of samples respectively. Nuclear staining was observed in 54.8% of cases for DVL1 and 53.3% for DVL3. The main effector of the Wnt signaling, beta-catenin, was up-regulated in 56%, and transferred to the nucleus in 36% of metastases. When DVL1 and DVL3 were up-regulated the number of cases with nuclear beta-catenin significantly increased (p=0.0001). Down-regulation of E-cadherin was observed in 80% of samples. Genetic analysis showed 36% of samples with LOH of the CDH1. In comparison to other lung cancer pathologies, the diagnoses adenocarcinoma and small cell lung cancer (SCLC) were significantly associated to CDH1 LOH (p=0.001). Microsatellite instability was detected in one metastasis from adenocarcinoma. Exon 3 of beta-catenin was not targeted. Altered expression of Dishevelled-1, Dishevelled-3, E-cadherin and beta-catenin were present in brain metastases which indicates that Wnt signaling is important and may contribute to better understanding of genetic profile conditioning lung cancer metastasis to the brain.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA


Projekti:
108-1081870-1905 - Uloga signalnog puta wnt u tumorigenezi i embriogenezi mozga (Pećina-Šlaus, Nives, MZOS ) ( CroRIS)

Ustanove:
Klinička bolnica "Merkur",
Medicinski fakultet, Zagreb,
KBC "Sestre Milosrdnice"

Profili:

Avatar Url Anja Kafka (autor)

Avatar Url Hrvoje Ivan Pećina (autor)

Avatar Url Vili Beroš (autor)

Avatar Url Davor Tomas (autor)

Poveznice na cjeloviti tekst rada:

doi www.mdpi.com

Citiraj ovu publikaciju:

Kafka, Anja; Tomas, Davor; Beroš, Vili; Pećina, Hrvoje Ivan; Zeljko, Martina; Pećina-Šlaus, Nives
Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin // International journal of molecular sciences, 15 (2014), 6; 10635-10651 doi:10.3390/ijms150610635 (međunarodna recenzija, članak, znanstveni)
Kafka, A., Tomas, D., Beroš, V., Pećina, H., Zeljko, M. & Pećina-Šlaus, N. (2014) Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin. International journal of molecular sciences, 15 (6), 10635-10651 doi:10.3390/ijms150610635.
@article{article, author = {Kafka, Anja and Tomas, Davor and Bero\v{s}, Vili and Pe\'{c}ina, Hrvoje Ivan and Zeljko, Martina and Pe\'{c}ina-\v{S}laus, Nives}, year = {2014}, pages = {10635-10651}, DOI = {10.3390/ijms150610635}, keywords = {Dishevelled-1 (DVL1), Dishevelled-3 (DVL3), E-cadherin (CDH1), beta-catenin (CTNNB1), brain metastases, lung cancer, immunostaining, loss of heterozygosity}, journal = {International journal of molecular sciences}, doi = {10.3390/ijms150610635}, volume = {15}, number = {6}, issn = {1422-0067}, title = {Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin}, keyword = {Dishevelled-1 (DVL1), Dishevelled-3 (DVL3), E-cadherin (CDH1), beta-catenin (CTNNB1), brain metastases, lung cancer, immunostaining, loss of heterozygosity} }
@article{article, author = {Kafka, Anja and Tomas, Davor and Bero\v{s}, Vili and Pe\'{c}ina, Hrvoje Ivan and Zeljko, Martina and Pe\'{c}ina-\v{S}laus, Nives}, year = {2014}, pages = {10635-10651}, DOI = {10.3390/ijms150610635}, keywords = {Dishevelled-1 (DVL1), Dishevelled-3 (DVL3), E-cadherin (CDH1), beta-catenin (CTNNB1), brain metastases, lung cancer, immunostaining, loss of heterozygosity}, journal = {International journal of molecular sciences}, doi = {10.3390/ijms150610635}, volume = {15}, number = {6}, issn = {1422-0067}, title = {Brain metastases from lung cancer show increased expression of DVL1, DVL3 and beta-catenin and down regulation of E-cadherin}, keyword = {Dishevelled-1 (DVL1), Dishevelled-3 (DVL3), E-cadherin (CDH1), beta-catenin (CTNNB1), brain metastases, lung cancer, immunostaining, loss of heterozygosity} }

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


Uključenost u ostale bibliografske baze podataka::


  • MEDLINE
  • Scopus
  • PubMed Central
  • Swiss national Library
  • google scholar


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