نتایج جستجو برای: ژن hoxb13

تعداد نتایج: 15960  

2016
Jingjing Liu Wendy J. C. Prager–van der Smissen Marjanka K. Schmidt J. Margriet Collée Sten Cornelissen Roy Lamping Anja Nieuwlaat John A. Foekens Maartje J. Hooning Senno Verhoef Ans M. W. van den Ouweland Frans B. L. Hogervorst John W. M. Martens Antoinette Hollestelle

The HOXB13 p.G84E mutation has been firmly established as a prostate cancer susceptibility allele. Although HOXB13 also plays a role in breast tumor progression, the association of HOXB13 p.G84E with breast cancer risk is less evident. Therefore, we comprehensively interrogated the entire HOXB13 coding sequence for mutations in 1,250 non-BRCA1/2 familial breast cancer cases and 800 controls. We...

2017
Ilka Kristiansen Carsten Stephan Klaus Jung Manfred Dietel Anja Rieger Yuri Tolkach Glen Kristiansen

AIMS Determining the origin of metastases is an important task of pathologists to allow for the initiation of a tumor-specific therapy. Recently, homeobox protein Hox-B13 (HOXB13) has been suggested as a new marker for the detection of prostatic origin. The aim of this study was to evaluate the diagnostic sensitivity of HOXB13 in comparison to commonly used immunohistochemical markers for prost...

2015
Hong Yuan Hiroaki Kajiyama Satoko Ito Dan Chen Kiyosumi Shibata Michinari Hamaguchi Fumitaka Kikkawa Takeshi Senga

Homeoproteins, a family of transcription factors that have conserved homeobox domains, play critical roles in embryonic development in a wide range of species. Accumulating studies have revealed that homeoproteins are aberrantly expressed in multiple tumors and function as either tumor promoters or suppressors. In this study, we show that two homeoproteins, HOXB13 and ALX4, are associated with ...

Journal: :Cancer research 2016
Gretchen K Hubbard Laura N Mutton May Khalili Ryan P McMullin Jessica L Hicks Daniella Bianchi-Frias Lucas A Horn Ibrahim Kulac Michael S Moubarek Peter S Nelson Srinivasan Yegnasubramanian Angelo M De Marzo Charles J Bieberich

Genetic instability, a hallmark feature of human cancers including prostatic adenocarcinomas, is considered a driver of metastasis. Somatic copy number alterations (CNA) are found in most aggressive primary human prostate cancers, and the overall number of such changes is increased in metastases. Chromosome 10q23 deletions, encompassing PTEN, and amplification of 8q24, harboring MYC, are freque...

2010
Kalpana Ghoshal Tasneem Motiwala Rainer Claus Pearlly Yan Huban Kutay Jharna Datta Sarmila Majumder Shoumei Bai Arnab Majumder Tim Huang Christoph Plass Samson T. Jacob

BACKGROUND A hallmark of cancer cells is hypermethylation of CpG islands (CGIs), which probably arises from upregulation of one or more DNA methyltransferases. The purpose of this study was to identify the targets of DNMT3B, an essential DNA methyltransferase in mammals, in colon cancer. METHODOLOGY/PRINCIPAL FINDINGS Chromatin immunoprecipitation with DNMT3B specific antibody followed by CGI...

2017
Tamara L. Lotan Alba Torres Miao Zhang Jeffrey J. Tosoian Liana B. Guedes Helen Fedor Jessica Hicks Charles M. Ewing Sarah D. Isaacs Dorhyun Johng Angelo M. De Marzo William B. Isaacs

A recurrent germline mutation (G84E) in the HOXB13 gene is associated with early onset and family history-positive prostate cancer in patients of European descent, occurring in up to 5% of prostate cancer families. To date, the molecular features of prostate tumors occurring in HOXB13 G84E carriers have not been studied in a large cohort of patients. We identified 101 heterozygous carriers of G...

Journal: :Cancer cell 2004
Dennis C Sgroi Daniel A Haber Paula D Ryan Xiao-Jun Ma Mark G Erlander

Tamoxifen significantly reduces tumor recurrence in certain patients with early-stage estrogen receptor-positive breast cancer, but markers predictive of treatment failure have not been identified. Here, we generated gene expression profiles of hormone receptor-positive primary breast cancers in a set of 60 patients treated with adjuvant tamoxifen monotherapy. An expression signature predictive...

2015
Ferras Albitar Kevin Diep Wanlong Ma Maher Albitar

BACKGROUND Genomic association and linkage studies, as well as epidemiological data have implicated both the HOXB13 gene and single nucleotide polymorphisms (SNPs) in the development of prostate cancer (PCa). The recent association between the G84E polymorphism in the HOXB13 gene and PCa has been shown to result in a more aggressive cancer with an earlier onset of the disease. We examined the f...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2006
Matthew P Goetz Vera J Suman James N Ingle Andrea M Nibbe Dan W Visscher Carol A Reynolds Wilma L Lingle Mark Erlander Xiao-Jun Ma Dennis C Sgroi Edith A Perez Fergus J Couch

PURPOSE In the adjuvant treatment of estrogen receptor (ER)-positive breast cancer, additional markers are needed to identify women at high risk for recurrence. EXPERIMENTAL DESIGN We examined the association between the ratio of the homeobox 13 (HOXB13) to interleukin-17B receptor (IL-17BR) expression and the clinical outcomes of relapse and survival in women with ER-positive breast cancer e...

2016
Takahide Hayano Hiroshi Matsui Hirofumi Nakaoka Nobuaki Ohtake Kazuyoshi Hosomichi Kazuhiro Suzuki Ituro Inoue

Prostate cancer (PC) is the second most common cancer in men. Family history is the major risk factor for PC. Only two susceptibility genes were identified in PC, BRCA2 and HOXB13. A comprehensive search of germline variants for patients with PC has not been reported in Japanese families. In this study, we conducted exome sequencing followed by Sanger sequencing to explore responsible germline ...

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