Cargando…

Variants of SCARB1 and VDR Involved in Complex Genetic Interactions May Be Implicated in the Genetic Susceptibility to Clear Cell Renal Cell Carcinoma

The current data are still inconclusive in terms of a genetic component involved in the susceptibility to renal cell carcinoma. Our aim was to evaluate 40 selected candidate polymorphisms for potential association with clear cell renal cell carcinoma (ccRCC) based on independent group of 167 patient...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pośpiech, Ewelina, Ligęza, Janusz, Wilk, Wacław, Gołas, Aniela, Jaszczyński, Janusz, Stelmach, Andrzej, Ryś, Janusz, Blecharczyk, Aleksandra, Wojas-Pelc, Anna, Jura, Jolanta, Branicki, Wojciech
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402472/ https://www.ncbi.nlm.nih.gov/pubmed/25945350 http://dx.doi.org/10.1155/2015/860405

Ejemplares similares

MCPIP1 contributes to clear cell renal cell carcinomas development
por: Ligeza, Janusz, et al.
Publicado: (2017)

MCPIP1 inhibits Wnt/β-catenin signaling pathway activity and modulates epithelial-mesenchymal transition during clear cell renal cell carcinoma progression by targeting miRNAs
por: Gorka, Judyta, et al.
Publicado: (2021)

Post-Irradiation Bladder Syndrome After Radiotherapy of Malignant Neoplasm of Small Pelvis Organs: An Observational, Non-Interventional Clinical Study Assessing VESIcare(®)/Solifenacin Treatment Results
por: Jaszczyński, Janusz, et al.
Publicado: (2016)

Further evidence for population specific differences in the effect of DNA markers and gender on eye colour prediction in forensics
por: Pośpiech, Ewelina, et al.
Publicado: (2016)

The intraoperative assessment of the effectiveness of computed tomography in the detection of the residual mass of the retroperitoneal space in patients with nonseminoma testicular tumors after chemotherapy
por: Jaszczyński, Janusz, et al.
Publicado: (2011)

Model-based prediction of human hair color using DNA variants
por: Branicki, Wojciech, et al.
Publicado: (2011)

Activity of MCPIP1 RNase in tumor associated processes
por: Miekus, Katarzyna, et al.
Publicado: (2019)

Degree of Enhancement on Contrast Enhanced Spectral Mammography (CESM) and Lesion Type on Mammography (MG): Comparison Based on Histological Results
por: Łuczyńska, Elżbieta, et al.
Publicado: (2016)

Irradiation-induced bone sarcoma in a patient treated for cervix cancer 28 years earlier
por: Klimek, Małgorzata, et al.
Publicado: (2012)

Resistance to tyrosine kinase inhibitors promotes renal cancer progression through MCPIP1 tumor-suppressor downregulation and c-Met activation
por: Marona, Paulina, et al.
Publicado: (2022)

Mucinous breast cancer – clinical characteristics and treatment results in patients treated at the Oncology Centre in Kraków between 1952 and 2002
por: Sas-Korczyńska, Beata, et al.
Publicado: (2014)

Prediction of eye color in the Slovenian population using the IrisPlex SNPs
por: Kastelic, Vanja, et al.
Publicado: (2013)

Vitamin D May Protect against Breast Cancer through the Regulation of Long Noncoding RNAs by VDR Signaling
por: Blasiak, Janusz, et al.
Publicado: (2022)

Genetic Variability in DNA Repair Proteins in Age-Related Macular Degeneration
por: Blasiak, Janusz, et al.
Publicado: (2012)

What's New in the Pathophysiology of Alopecia Areata? The Possible Contribution of Skin and Gut Microbiome in the Pathogenesis of Alopecia – Big Opportunities, Big Challenges, and Novel Perspectives
por: Migacz-Gruszka, Kamila, et al.
Publicado: (2019)

Predicting Physical Appearance from DNA Data—Towards Genomic Solutions
por: Pośpiech, Ewelina, et al.
Publicado: (2022)

Effects of host genetic variations on response to, susceptibility and severity of respiratory infections
por: Ghafouri-Fard, Soudeh, et al.
Publicado: (2020)

RNA sequencing reveals widespread transcriptome changes in a renal carcinoma cell line
por: Lichawska-Cieslar, Agata, et al.
Publicado: (2018)

Prognostic Significance of Serum PSA Level and Telomerase, VEGF and GLUT-1 Protein Expression for the Biochemical Recurrence in Prostate Cancer Patients after Radical Prostatectomy
por: Gasinska, Anna, et al.
Publicado: (2019)

Bona fide colour: DNA prediction of human eye and hair colour from ancient and contemporary skeletal remains
por: Draus-Barini, Jolanta, et al.
Publicado: (2013)

Pathological complete response after cisplatin neoadjuvant therapy is associated with the downregulation of DNA repair genes in BRCA1-associated triple-negative breast cancers
por: Domagala, Pawel, et al.
Publicado: (2016)

Complex Structural Effects in Deformed High-Manganese Steel
por: Kowalska, Joanna, et al.
Publicado: (2021)

Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study
por: Niemsiri, Vipavee, et al.
Publicado: (2015)

Association of genetic polymorphisms of GALNT3 and VDR with osteoporosis in postmenopausal women
por: Wang, Guorong, et al.
Publicado: (2016)

The Significance of VDR Genetic Polymorphisms in the Etiology of Preeclampsia in Pregnant Polish Women
por: Magiełda-Stola, Justyna, et al.
Publicado: (2021)

Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features
por: Hopfner, Franziska, et al.
Publicado: (2011)

Genetic polymorphism of the iron-regulatory protein-1 and -2 genes in age-related macular degeneration
por: Synowiec, Ewelina, et al.
Publicado: (2012)

Bridging the gap between clear cell renal cell carcinoma and cutaneous melanoma: the role of SCARB1 in dysregulated cholesterol metabolism
por: Song, Lebin, et al.
Publicado: (2023)

Genetic Influences on Response to Mood Stabilizers in Bipolar Disorder: Current Status of Knowledge
por: Rybakowski, Janusz K.
Publicado: (2013)

SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease
por: Alcalay, Roy N, et al.
Publicado: (2016)

SCARB1 downregulation in adrenal insufficiency with Allgrove syndrome
por: Bitetto, Giacomo, et al.
Publicado: (2023)

Patient selection in genetic association studies in idiopathic scoliosis
por: Harasymczuk, P, et al.
Publicado: (2013)

The influence of different culture microenvironments on the generation of dendritic cells from non-small-cell lung cancer patients
por: Krawczyk, Paweł, et al.
Publicado: (2007)

Vitamin D Receptor (VDR) Genetic Variants: Relationship of FokI Genotypes with VDR Expression and Clinical Disease Activity in Systemic Lupus Erythematosus Patients
por: Meza-Meza, Mónica R., et al.
Publicado: (2022)

Loss of epidermal MCPIP1 is associated with aggressive squamous cell carcinoma
por: Szukala, Weronika, et al.
Publicado: (2021)

Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor Retardation
por: Pasińska, Magdalena, et al.
Publicado: (2022)

Genetic aspects of idiopathic scoliosis – literature review
por: Janusz, P, et al.
Publicado: (2012)

Prognostic Role of Tumoral PD-L1 and IDO1 Expression, and Intratumoral CD8+ and FoxP3+ Lymphocyte Infiltrates in 132 Primary Cutaneous Merkel Cell Carcinomas
por: Donizy, Piotr, et al.
Publicado: (2021)

Integration of VDR genome wide binding and GWAS genetic variation data reveals co-occurrence of VDR and NF-κB binding that is linked to immune phenotypes
por: Singh, Prashant K., et al.
Publicado: (2017)

Vitamin D Status and Association of VDR Genetic Polymorphism to Risk of Breast Cancer in Ethiopia
por: Ahmed, Jemal Hussien, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_9giig5ldmddo60187qa9csosaj