Literature DB >> 17990101

JAG1 expression is associated with a basal phenotype and recurrence in lymph node-negative breast cancer.

Michael Reedijk1, Dushanthi Pinnaduwage, Brendan C Dickson, Anna Marie Mulligan, Hui Zhang, Shelley B Bull, Frances P O'Malley, Sean E Egan, Irene L Andrulis.   

Abstract

Expression of the JAG1 Notch ligand has previously been shown to correlate with poor overall survival in women with advanced breast cancer. We undertook to test whether expression of JAG1 is associated with reduced disease free survival (DFS) in 887 samples from a prospectively accrued LNN cohort with a median follow-up greater than 8 years. Moderate to high JAG1 mRNA expression was associated with reduced DFS in univariate analysis (hazard ratio of 1.58; 95% confidence interval, 1.03-2.40; P = 0.034) and correlated with large tumor size, ER and PgR negativity, high tumor grade, and p53 antibody reactivity. Although elevated risk of reduced DFS in patients with high JAG1 mRNA did not persist with adjustment for other prognostic factors, it did in combination with HER2. JAG1 mRNA was positively associated with expression of basal breast cancer markers, however, in contrast to the finding that basal gene expression is most strongly associated with reduced DFS in the first 36 months of follow-up, JAG1 mRNA expression was associated with reduced DFS through the full follow-up period. Also, tumors expressing high levels of both mRNA and protein showed reduced DFS as compared to all other groups in univariate analysis (hazard ratio of 1.73; 95% confidence interval, 1.09-2.74; P = 0.020). Thus, JAG1 expression is associated with poor DFS in LNN breast cancer. As JAG1 is a target of several oncogenic signaling pathways, and is a ligand for Notch, these data provide novel insights into signaling that may contribute to progression of early stage breast cancer.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17990101     DOI: 10.1007/s10549-007-9805-3

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  70 in total

Review 1.  Two Sides of the Same Coin: The Role of Developmental pathways and pluripotency factors in normal mammary stem cells and breast cancer metastasis.

Authors:  M U J Oliphant; Deguang Kong; Hengbo Zhou; M T Lewis; H L Ford
Journal:  J Mammary Gland Biol Neoplasia       Date:  2020-04-22       Impact factor: 2.673

Review 2.  Notch as a tumour suppressor.

Authors:  Craig S Nowell; Freddy Radtke
Journal:  Nat Rev Cancer       Date:  2017-02-03       Impact factor: 60.716

3.  Quantitative DNA hypomethylation of ligand Jagged1 and receptor Notch1 signifies occurrence and progression of breast carcinoma.

Authors:  Yuwen Cao; Yixiao Li; Na Zhang; Jianming Hu; Liang Yin; Zemin Pan; Yucong Li; Xiaoming Du; Wenjie Zhang; Feng Li
Journal:  Am J Cancer Res       Date:  2015-04-15       Impact factor: 6.166

Review 4.  Cross-talk between miRNA and Notch signaling pathways in tumor development and progression.

Authors:  Zhiwei Wang; Yiwei Li; Dejuan Kong; Aamir Ahmad; Sanjeev Banerjee; Fazlul H Sarkar
Journal:  Cancer Lett       Date:  2009-12-22       Impact factor: 8.679

5.  The ZEB1/miR-200 feedback loop controls Notch signalling in cancer cells.

Authors:  Simone Brabletz; Karolina Bajdak; Simone Meidhof; Ulrike Burk; Gabriele Niedermann; Elke Firat; Ulrich Wellner; Arno Dimmler; Gerhard Faller; Jörg Schubert; Thomas Brabletz
Journal:  EMBO J       Date:  2011-01-11       Impact factor: 11.598

6.  Targeting Met and Notch in the Lfng-deficient, Met-amplified triple-negative breast cancer.

Authors:  Shubing Zhang; Wen-cheng Chung; Lucio Miele; Keli Xu
Journal:  Cancer Biol Ther       Date:  2014-02-20       Impact factor: 4.742

Review 7.  The Notch signaling pathway as a mediator of tumor survival.

Authors:  Kathleen M Capaccione; Sharon R Pine
Journal:  Carcinogenesis       Date:  2013-04-12       Impact factor: 4.944

8.  Notch-1 activates estrogen receptor-alpha-dependent transcription via IKKalpha in breast cancer cells.

Authors:  L Hao; P Rizzo; C Osipo; A Pannuti; D Wyatt; L W-K Cheung; G Sonenshein; B A Osborne; L Miele
Journal:  Oncogene       Date:  2009-10-19       Impact factor: 9.867

9.  Expression profiling of familial breast cancers demonstrates higher expression of FGFR2 in BRCA2-associated tumors.

Authors:  Anita L Bane; Dushanthi Pinnaduwage; Sarah Colby; Michael Reedijk; Sean E Egan; Shelley B Bull; Frances P O'Malley; Irene L Andrulis
Journal:  Breast Cancer Res Treat       Date:  2008-06-18       Impact factor: 4.872

10.  Characterization of Notch1 antibodies that inhibit signaling of both normal and mutated Notch1 receptors.

Authors:  Miguel Aste-Amézaga; Ningyan Zhang; Janet E Lineberger; Beth A Arnold; Timothy J Toner; Mingcheng Gu; Lingyi Huang; Salvatore Vitelli; Kim T Vo; Peter Haytko; Jing Zhang Zhao; Frederic Baleydier; Sarah L'Heureux; Hongfang Wang; Wendy R Gordon; Elizabeth Thoryk; Marie Blanke Andrawes; Kittichoat Tiyanont; Kimberly Stegmaier; Giovanni Roti; Kenneth N Ross; Laura L Franlin; Hui Wang; Fubao Wang; Michael Chastain; Andrew J Bett; Laurent P Audoly; Jon C Aster; Stephen C Blacklow; Hans E Huber
Journal:  PLoS One       Date:  2010-02-08       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.