Analysis of A Disintegrin and Metalloprotease 17 (ADAM17) Expression as a Prognostic Marker in Ovarian Cancer Patients Undergoing First-Line Treatment Plus Bevacizumab
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A. Gadducci | S. Pignata | V. Canzonieri | G. Scognamiglio | D. Califano | N. Colombo | G. Scambia | S. Ferrini | S. Signoriello | F. Perrone | P. Chiodini | D. Mezzanzanica | M. Bagnoli | G. Filaci | D. Russo | M. Fabbi | A. Spina | C. Pisano | L. Arenare | N. Losito | D. Costa | G. Gaggero | Delfina Costa
[1] W. Lieb,et al. ADAM17—A Potential Blood-Based Biomarker for Detection of Early-Stage Ovarian Cancer , 2021, Cancers.
[2] S. Pignata,et al. Evaluation of Angiogenesis-Related Genes as Prognostic Biomarkers of Bevacizumab Treated Ovarian Cancer Patients: Results from the Phase IV MITO16A/ManGO OV-2 Translational Study , 2021, Cancers.
[3] D. Katsaros,et al. Bevacizumab, carboplatin, and paclitaxel in the first line treatment of advanced ovarian cancer patients: the phase IV MITO-16A/MaNGO-OV2A study , 2021, International Journal of Gynecological Cancer.
[4] S. Sebens,et al. ADAM17 Inhibition Increases the Impact of Cisplatin Treatment in Ovarian Cancer Spheroids , 2021, Cancers.
[5] S. Pignata,et al. Ovarian Cancer Translational Activity of the Multicenter Italian Trial in Ovarian Cancer (MITO) Group: Lessons Learned in 10 Years of Experience , 2020, Cells.
[6] Junfa Li,et al. Reciprocal control of ADAM17/EGFR/Akt signaling and miR-145 drives GBM invasiveness , 2020, Journal of Neuro-Oncology.
[7] F. Marmé,et al. Olaparib plus Bevacizumab as First-Line Maintenance in Ovarian Cancer. , 2019, The New England journal of medicine.
[8] D. Longo. Personalized Medicine for Primary Treatment of Serous Ovarian Cancer. , 2019, The New England journal of medicine.
[9] A. Marchetti,et al. Recommendations for the implementation of BRCA testing in ovarian cancer patients and their relatives. , 2019, Critical reviews in oncology/hematology.
[10] Danielle M. Enserro,et al. Final Overall Survival of a Randomized Trial of Bevacizumab for Primary Treatment of Ovarian Cancer. , 2019, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[11] C. Garbers,et al. The metalloprotease ADAM17 in inflammation and cancer. , 2019, Pathology, research and practice.
[12] Qiuping Xu,et al. NOTCH2/NOTCH3/DLL3/MAML1/ADAM17 signaling network is associated with ovarian cancer , 2019, Oncology letters.
[13] A. Gavin,et al. Cancer incidence and mortality patterns in Europe: Estimates for 40 countries and 25 major cancers in 2018. , 2018, European journal of cancer.
[14] Guo-Dong Wang,et al. ADAM17 promotes cell migration and invasion through the integrin &bgr;1 pathway in hepatocellular carcinoma , 2018, Experimental cell research.
[15] Ying Chen,et al. ADAM-17 is a poor prognostic indicator for patients with hilar cholangiocarcinoma and is regulated by FoxM1 , 2018, BMC cancer.
[16] D. Schmidt-Arras,et al. ADAM17 inhibition enhances platinum efficiency in ovarian cancer , 2018, Oncotarget.
[17] Ying Chen,et al. ADAM-17 expression is enhanced by FoxM1 and is a poor prognostic sign in gastric carcinoma. , 2017, The Journal of surgical research.
[18] Huirong Shi,et al. Long non‐coding RNA CCAT1 promotes metastasis and poor prognosis in epithelial ovarian cancer , 2017, Experimental cell research.
[19] A. Skubitz,et al. Ectodomain shedding of the cell adhesion molecule Nectin-4 in ovarian cancer is mediated by ADAM10 and ADAM17 , 2017, The Journal of Biological Chemistry.
[20] S. Ferrini,et al. Targeting ADAM17 Sheddase Activity in Cancer. , 2016, Current drug targets.
[21] G. Mills,et al. An antibody to amphiregulin, an abundant growth factor in patients’ fluids, inhibits ovarian tumors , 2016, Oncogene.
[22] Jacobus Pfisterer,et al. Standard chemotherapy with or without bevacizumab for women with newly diagnosed ovarian cancer (ICON7): overall survival results of a phase 3 randomised trial , 2015, The Lancet. Oncology.
[23] M. Swartz,et al. ADAM17 Promotes Motility, Invasion, and Sprouting of Lymphatic Endothelial Cells , 2015, PloS one.
[24] X. Zhang,et al. Expression and clinical significance of ADAM17 protein in esophageal squamous cell carcinoma. , 2015, Genetics and molecular research : GMR.
[25] A. Bilici,et al. Prognostic significance of ADAM17 expression in patients with gastric cancer who underwent curative gastrectomy , 2015, Clinical and Translational Oncology.
[26] M. Péoc'h,et al. A novel marker ADAM17 for clear cell renal cell carcinomas: implication for patients' prognosis. , 2014, Urologic oncology.
[27] Hong-Bin Liu,et al. A disintegrin and metalloproteinase 17 mRNA and protein expression in esophageal squamous cell carcinoma, as well as its clinicopathological factors and prognosis , 2014, Molecular medicine reports.
[28] A. Chalaris,et al. ADAM10 and ADAM17 have opposite roles during sprouting angiogenesis , 2014, Angiogenesis.
[29] Ying Chen,et al. Differential expression of ANXA1 in benign human gastrointestinal tissues and cancers , 2014, BMC Cancer.
[30] Mingang Ying,et al. ADAM17 is associated with EMMPRIN and predicts poor prognosis in patients with uterine cervical carcinoma , 2014, Tumor Biology.
[31] Ji Zhang,et al. ADAM17 is overexpressed in non-small cell lung cancer and its expression correlates with poor patient survival , 2013, Tumor Biology.
[32] M. Swartz,et al. ADAM17 Silencing in Mouse Colon Carcinoma Cells: The Effect on Tumoricidal Cytokines and Angiogenesis , 2012, PloS one.
[33] Zhong-sheng Zhao,et al. Upregulated Expression of ADAM17 Is a Prognostic Marker for Patients With Gastric Cancer , 2012, Annals of surgery.
[34] Wei-Guo Zhu,et al. Prognostic value of ADAM17 in human gastric cancer , 2012, Medical Oncology.
[35] A. Harris,et al. The unfolded protein response controls induction and activation of ADAM17/TACE by severe hypoxia and ER stress , 2012, Oncogene.
[36] D. Jodrell,et al. Anti-Tumour Effects of a Specific Anti-ADAM17 Antibody in an Ovarian Cancer Model In Vivo , 2012, PloS one.
[37] M. Chopp,et al. ADAM17 promotes glioma cell malignant phenotype , 2012, Molecular carcinogenesis.
[38] A. Anghel,et al. Increased expression of ADAM12 and ADAM17 genes in laser-capture microdissected breast cancers and correlations with clinical and pathological characteristics. , 2012, Acta histochemica.
[39] B. Monk,et al. Incorporation of bevacizumab in the primary treatment of ovarian cancer. , 2011, The New England journal of medicine.
[40] Jacobus Pfisterer,et al. A phase 3 trial of bevacizumab in ovarian cancer. , 2011, The New England journal of medicine.
[41] Stefan Rose-John,et al. ADAM17: a molecular switch to control inflammation and tissue regeneration. , 2011, Trends in immunology.
[42] G. Mills,et al. Somatic mutations in BRCA1 and BRCA2 could expand the number of patients that benefit from poly (ADP ribose) polymerase inhibitors in ovarian cancer. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[43] K. Horiuchi,et al. Pathological Neovascularization Is Reduced by Inactivation of ADAM17 in Endothelial Cells but Not in Pericytes , 2010, Circulation research.
[44] M. Gooz. ADAM-17: the enzyme that does it all , 2010, Critical reviews in biochemistry and molecular biology.
[45] J. Arribas,et al. ADAM17 as a therapeutic target in multiple diseases. , 2009, Current pharmaceutical design.
[46] F. Bolster,et al. ADAM-17 predicts adverse outcome in patients with breast cancer. , 2008, Annals of oncology : official journal of the European Society for Medical Oncology.
[47] J. Bartlett,et al. Expression of tumor necrosis factor alpha converting enzyme in endocrine cancers. , 2008, American Journal of Clinical Pathology.
[48] B. LaFleur,et al. TACE/ADAM-17: A Component of the Epidermal Growth Factor Receptor Axis and a Promising Therapeutic Target in Colorectal Cancer , 2008, Clinical Cancer Research.
[49] S. Canevari,et al. The ALCAM Shedding by the Metalloprotease ADAM17/TACE Is Involved in Motility of Ovarian Carcinoma Cells , 2007, Molecular Cancer Research.
[50] P. Kenny. TACE: a new target in epidermal growth factor receptor dependent tumors. , 2007, Differentiation; research in biological diversity.
[51] A. Reeve,et al. Genome wide expression profiling identifies genes associated with colorectal liver metastasis. , 2007, Oncology reports.
[52] Satoshi O. Suzuki,et al. Clinical Significance of Heparin-Binding Epidermal Growth Factor–Like Growth Factor and A Disintegrin and Metalloprotease 17 Expression in Human Ovarian Cancer , 2005, Clinical Cancer Research.
[53] W. Sauerbrei,et al. Confidence intervals for the effect of a prognostic factor after selection of an ‘optimal’ cutpoint , 2004, Statistics in medicine.
[54] G. Weskamp,et al. Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands , 2004, The Journal of cell biology.
[55] J. Baselga,et al. TACE is required for the activation of the EGFR by TGF‐α in tumors , 2003 .
[56] C. Osborne,et al. Immunoreactive alpha transforming growth factor activity in effusions from cancer patients as a marker of tumor burden and patient prognosis. , 1988, Cancer research.
[57] J. Ledermann,et al. ESGO consensus conference recommendations on ovarian cancer : pathology and molecular biology , early and advanced stages , borderline tumours and recurrent disease , 2019 .
[58] C. Blobel,et al. ADAMs: key components in EGFR signalling and development , 2005, Nature Reviews Molecular Cell Biology.
[59] J. Baselga,et al. TACE is required for the activation of the EGFR by TGF-alpha in tumors. , 2003, The EMBO journal.
[60] A. Ullrich,et al. EGF receptor transactivation by G-protein-coupled receptors requires metalloproteinase cleavage of proHB-EGF , 1999, Nature.