Accès à distance ? S'identifier sur le proxy UCLouvain
Novel highly specific anti-periostin antibodies uncover the functional importance of the fascilin 1-1 domain and highlight preferential expression of periostin in aggressive breast cancer.
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Document type | Article de périodique (Journal article) – Article de recherche |
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Access type | Accès interdit |
Publication date | 2016 |
Language | Anglais |
Journal information | "International Journal of Cancer" - Vol. 138, no. 8, p. 1959-1970 (2016) |
Peer reviewed | yes |
Publisher | Wiley-Liss ((United States) New York, NY) |
issn | 0020-7136 |
e-issn | 1097-0215 |
Publication status | Publié |
Affiliations |
UCL
- SSS/DDUV/MEXP - Médecine expérimentale UCL - SSS/IONS - Institute of NeuroScience UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire |
MESH Subject | Adult ; Breast Neoplasms ; Cell Adhesion Molecules ; Cell Movement ; Female ; Humans ; Immunohistochemistry ; Mice ; Middle Aged ; Tissue Array Analysis ; Aged ; Aged, 80 and over ; Amino Acid Motifs ; Animals ; Antibodies, Monoclonal ; Antibody Specificity ; Binding Sites, Antibody ; Biomarkers, Tumor |
Keywords | FAS1-1 domain ; Breast cancer ; Diagnostic marker ; Extracellular matrix protein ; Monoclonal antibodies ; Periostin |
Links |
- Takeshita S, Kikuno R, Tezuka K, Amann E, Osteoblast-specific factor 2: cloning of a putative bone adhesion protein with homology with the insect protein fasciclin I, 10.1042/bj2940271
- Hoersch Sebastian, Andrade-Navarro Miguel A, Periostin shows increased evolutionary plasticity in its alternatively spliced region, 10.1186/1471-2148-10-30
- Zinn Kai, McAllister Linda, Goodman Corey S., Sequence analysis and neuronal expression of fasciclin I in grasshopper and drosophila, 10.1016/0092-8674(88)90574-0
- Morra Laura, Moch Holger, Periostin expression and epithelial-mesenchymal transition in cancer: a review and an update, 10.1007/s00428-011-1151-5
- Kudo Akira, Periostin in fibrillogenesis for tissue regeneration: periostin actions inside and outside the cell, 10.1007/s00018-011-0784-5
- Desgrosellier Jay S., Cheresh David A., Integrins in cancer: biological implications and therapeutic opportunities, 10.1038/nrc2748
- Seguin Laetitia, Kato Shumei, Franovic Aleksandra, Camargo M. Fernanda, Lesperance Jacqueline, Elliott Kathryn C., Yebra Mayra, Mielgo Ainhoa, Lowy Andrew M., Husain Hatim, Cascone Tina, Diao Lixia, Wang Jing, Wistuba Ignacio I., Heymach John V., Lippman Scott M., Desgrosellier Jay S., Anand Sudarshan, Weis Sara M., Cheresh David A., An integrin β3–KRAS–RalB complex drives tumour stemness and resistance to EGFR inhibition, 10.1038/ncb2953
- Desgrosellier Jay S., Lesperance Jacqueline, Seguin Laetitia, Gozo Maricel, Kato Shumei, Franovic Aleksandra, Yebra Mayra, Shattil Sanford J., Cheresh David A., Integrin αvβ3 Drives Slug Activation and Stemness in the Pregnant and Neoplastic Mammary Gland, 10.1016/j.devcel.2014.06.005
- Liapis Helen, Flath Alanna, Kitazawa Sohei, Integrin αvβ3 Expression by Bone-residing Breast Cancer Metastases : , 10.1097/00019606-199606000-00008
- Takayama, Anticancer Res, 25, 79 (2005)
- Dorn Gerald W., Periostin and Myocardial Repair, Regeneration, and Recovery, 10.1056/nejmcibr074816
- Takayama Go, Arima Kazuhiko, Kanaji Taisuke, Toda Shuji, Tanaka Hiroyuki, Shoji Shunsuke, McKenzie Andrew N.J., Nagai Hiroichi, Hotokebuchi Takao, Izuhara Kenji, Periostin: A novel component of subepithelial fibrosis of bronchial asthma downstream of IL-4 and IL-13 signals, 10.1016/j.jaci.2006.02.046
- Grigoriadis Anita, Mackay Alan, Reis-Filho Jorge S, Steele Dawn, Iseli Christian, Stevenson Brian J, Jongeneel C Victor, Valgeirsson Haukur, Fenwick Kerry, Iravani Marjan, Leao Maria, Simpson Andrew JG, Strausberg Robert L, Jat Parmjit S, Ashworth Alan, Neville A Munro, O'Hare Michael J, Establishment of the epithelial-specific transcriptome of normal and malignant human breast cells based on MPSS and array expression data, 10.1186/bcr1604
- Bao Shideng, Ouyang Gaoliang, Bai Xuefang, Huang Zhi, Ma Chaoyu, Liu Ming, Shao Rong, Anderson Ryan M, Rich Jeremy N, Wang Xiao-Fan, Periostin potently promotes metastatic growth of colon cancer by augmenting cell survival via the Akt/PKB pathway, 10.1016/s1535-6108(04)00081-9
- Baril P, Gangeswaran R, Mahon P C, Caulee K, Kocher H M, Harada T, Zhu M, Kalthoff H, Crnogorac-Jurcevic T, Lemoine N R, Periostin promotes invasiveness and resistance of pancreatic cancer cells to hypoxia-induced cell death: role of the β4 integrin and the PI3k pathway, 10.1038/sj.onc.1210009
- Ismail, Cancer Res, 60, 6744 (2000)
- Gillan, Cancer Res, 62, 5358 (2002)
- Takanami I., Abiko T., Koizumi S., Expression of periostin in patients with non-small cell lung cancer: correlation with angiogenesis and lymphangiogenesis, 10.5301/jbm.2008.1999
- Kudo Yasusei, Ogawa Ikuko, Kitajima Shojiro, Kitagawa Masae, Kawai Hidehiko, Gaffney Patrick M., Miyauchi Mutsumi, Takata Takashi, Periostin Promotes Invasion and Anchorage-Independent Growth in the Metastatic Process of Head and Neck Cancer, 10.1158/0008-5472.can-05-4540
- Tilman Gaëlle, Mattiussi Marina, Brasseur Francis, van Baren Nicolas, Decottignies Anabelle, Human periostin gene expression in normal tissues, tumors and melanoma: evidences for periostin production by both stromal and melanoma cells, 10.1186/1476-4598-6-80
- Kikuchi Yoshinao, Kashima Takeshi G., Nishiyama Takashi, Shimazu Kazuhiro, Morishita Yasuyuki, Shimazaki Masashi, Kii Isao, Horie Hisanaga, Nagai Hideo, Kudo Akira, Fukayama Masashi, Periostin Is Expressed in Pericryptal Fibroblasts and Cancer-associated Fibroblasts in the Colon, 10.1369/jhc.2008.951061
- Malanchi Ilaria, Santamaria-Martínez Albert, Susanto Evelyn, Peng Hong, Lehr Hans-Anton, Delaloye Jean-Francois, Huelsken Joerg, Interactions between cancer stem cells and their niche govern metastatic colonization, 10.1038/nature10694
- Shao R., Bao S., Bai X., Blanchette C., Anderson R. M., Dang T., Gishizky M. L., Marks J. R., Wang X.-F., Acquired Expression of Periostin by Human Breast Cancers Promotes Tumor Angiogenesis through Up-Regulation of Vascular Endothelial Growth Factor Receptor 2 Expression, 10.1128/mcb.24.9.3992-4003.2004
- Baker A-M, Bird D, Lang G, Cox T R, Erler J T, Lysyl oxidase enzymatic function increases stiffness to drive colorectal cancer progression through FAK, 10.1038/onc.2012.202
- Zhou Wenchao, Ke Susan Q., Huang Zhi, Flavahan William, Fang Xiaoguang, Paul Jeremy, Wu Ling, Sloan Andrew E., McLendon Roger E., Li Xiaoxia, Rich Jeremy N., Bao Shideng, Periostin secreted by glioblastoma stem cells recruits M2 tumour-associated macrophages and promotes malignant growth, 10.1038/ncb3090
- Kalka, Res, 86, 1198 (2000)
- Kalka C., Masuda H., Takahashi T., Kalka-Moll W. M., Silver M., Kearney M., Li T., Isner J. M., Asahara T., Transplantation of ex vivo expanded endothelial progenitor cells for therapeutic neovascularization, 10.1073/pnas.97.7.3422
- Riley V., Lilly F., Huerto E., Bardell D., Transmissible Agent Associated with 26 Types of Experimental Mouse Neoplasms, 10.1126/science.132.3426.545
- Coutelier Jean-Paul, Van Snick Jacques, Isotypically restricted activation of B lymphocytes by lactic dehydrogenase virus, 10.1002/eji.1830150308
- Uyttenhove C., Marillier R. G., Tacchini-Cottier F., Charmoy M., Caspi R. R., Damsker J. M., Goriely S., Su D., Van Damme J., Struyf S., Opdenakker G., Van Snick J., Amine-reactive OVA multimers for auto-vaccination against cytokines and other mediators: perspectives illustrated for GCP-2 in L. major infection, 10.1189/jlb.1210699
- Gomez K. A., Coutelier J.-P., Retegui L. A., Changes in the Specificity of Antibodies in Mice Infected with Lactate Dehydrogenase-Elevating Virus, 10.1046/j.1365-3083.1997.d01-107.x
- Kogelberg Heide, Miranda Enrique, Burnet Jerome, Ellison David, Tolner Berend, Foster Julie, Picón Carmen, Thomas Gareth J., Meyer Tim, Marshall John F., Mather Stephen J., Chester Kerry, Generation and Characterization of a Diabody Targeting the αvβ6 Integrin, 10.1371/journal.pone.0073260
- Leavesley, IUBMB Life, 65, 807 (2013)
- Orecchia Paola, Conte Romana, Balza Enrica, Castellani Patrizia, Borsi Laura, Zardi Luciano, Mingari Maria Cristina, Carnemolla Barbara, Identification of a novel cell binding site of periostin involved in tumour growth, 10.1016/j.ejca.2011.04.026
- Kim Ba Reun, Jang Il Ho, Shin Sang Hun, Kwon Yang Woo, Heo Soon Chul, Choi Eun-Jung, Lee Jung Sub, Kim Jae Ho, Therapeutic angiogenesis in a murine model of limb ischemia by recombinant periostin and its fasciclin I domain, 10.1016/j.bbadis.2014.05.004
- Tai Isabella T., Dai Meiru, Chen Lan Bo, Periostin induction in tumor cell line explants and inhibition of in vitro cell growth by anti-periostin antibodies , 10.1093/carcin/bgi034
- Zhu M., Saxton R. E., Ramos L., Chang D. D., Karlan B. Y., Gasson J. C., Slamon D. J., Neutralizing Monoclonal Antibody to Periostin Inhibits Ovarian Tumor Growth and Metastasis, 10.1158/1535-7163.mct-11-0046
- Puglisi F, Puppin C, Pegolo E, Andreetta C, Pascoletti G, D'Aurizio F, Pandolfi M, Fasola G, Piga A, Damante G, Di Loreto C, Expression of periostin in human breast cancer, 10.1136/jcp.2007.052506
- Kim Jung-Eun, Jeong Ha-Won, Nam Ju-Ock, Lee Byung-Heon, Choi Je-Yong, Park Rang-Woon, Park Jae Yong, Kim In-San, Identification of Motifs in the Fasciclin Domains of the Transforming Growth Factor-β-induced Matrix Protein βig-h3 That Interact with the αvβ5 Integrin, 10.1074/jbc.m207055200
- Nam Ju-Ock, Kim Jung-Eun, Jeong Ha-Won, Lee Sung-Jin, Lee Byung-Heon, Choi Je-Yong, Park Rang-Woon, Park Jae Yong, Kim In-San, Identification of the αvβ3Integrin-interacting Motif of βig-h3 and Its Anti-angiogenic Effect, 10.1074/jbc.m300358200
Bibliographic reference | Field, Sarah ; Uyttenhove, Catherine ; Stroobant, Vincent ; Cheou, Paméla ; Donckers, Dominique ; et. al. Novel highly specific anti-periostin antibodies uncover the functional importance of the fascilin 1-1 domain and highlight preferential expression of periostin in aggressive breast cancer.. In: International Journal of Cancer, Vol. 138, no. 8, p. 1959-1970 (2016) |
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Permanent URL | http://hdl.handle.net/2078/179185 |