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      Expression of Periostin, Homologous with an Insect Cell Adhesion Molecule, as a Prognostic Marker in Non‐small Cell Lung Cancers

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          Abstract

          We used our palindromic polymerase chain reaction (PCR)‐driven cDNA differential display technique to identify and isolate a gene, designated periostin, from cancer tissues and found it to be overexpressed in several human tumors. We attempted to determine the influence of periostin expression on clinical outcome in patients with non‐small cell lung cancer (NSCLC) by reverse transcriptase (RT)‐PCR analysis. Periostin gene was highly expressed at the tumor periphery of lung cancer tissue but not within the tumor by in situ RNA hybridization, suggesting that expression of periostin may be involved in the process of tumor invasion. Periostin transcripts were detected in 50 (49.0%) of the tumor samples, although some paired normal lung samples showed weak expression. There was no relationship between periostin gene expression and gender, N‐ or T‐status. The NSCLC patients with periostin expression had significantly poorer survival than the patients without periostin expression ( P=0.0338).

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          Most cited references14

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          Revisions in the International System for Staging Lung Cancer.

          Revisions in stage grouping of the TNM subsets (T=primary tumor, N=regional lymph nodes, M=distant metastasis) in the International System for Staging Lung Cancer have been adopted by the American Joint Committee on Cancer and the Union Internationale Contre le Cancer. These revisions were made to provide greater specificity for identifying patient groups with similar prognoses and treatment options with the least disruption of the present classification: T1N0M0, stage IA; T2N0M0, stage IB; T1N1M0, stage IIA; T2N1M0 and T3N0M0, stage IIB; and T3N1M0, T1N2M0, T2N2M0, T3N2M0, stage IIIA. The TNM subsets in stage IIIB-T4 any N M0, any T N3M0, and in stage IV-any T any N M1, remain the same. Analysis of a collected database representing all clinical, surgical-pathologic, and follow-up information for 5,319 patients treated for primary lung cancer confirmed the validity of the TNM and stage grouping classification schema.
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            Metastases in carcinoma; analysis of 1000 autopsied cases.

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              A chemokine expressed in lymphoid high endothelial venules promotes the adhesion and chemotaxis of naive T lymphocytes.

              Preferential homing of naive lymphocytes to secondary lymphoid organs is thought to involve the action of chemokines, yet no chemokine has been shown to have either the expression pattern or the activities required to mediate this process. Here we show that a chemokine represented in the EST database, secondary lymphoid-tissue chemokine (SLC), is expressed in the high endothelial venules of lymph nodes and Peyer's patches, in the T cell areas of spleen, lymph nodes, and Peyer's patches, and in the lymphatic endothelium of multiple organs. SLC is a highly efficacious chemoattractant for lymphocytes with preferential activity toward naive T cells. Moreover, SLC induces firm adhesion of naive T lymphocytes via beta2 integrin binding to the counter receptor, intercellular adhesion molecule-1, a necessary step for lymphocyte recruitment. SLC is the first chemokine demonstrated to have the characteristics required to mediate homing of lymphocytes to secondary lymphoid organs. In addition, the expression of SLC in lymphatic endothelium suggests that the migration of lymphocytes from tissues into efferent lymphatics may be an active process mediated by this molecule.
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                Author and article information

                Journal
                Jpn J Cancer Res
                Jpn. J. Cancer Res
                10.1111/(ISSN)1349-7006a
                CAS
                Japanese Journal of Cancer Research : Gann
                Blackwell Publishing Ltd (Oxford, UK )
                0910-5050
                1876-4673
                August 2001
                : 92
                : 8 ( doiID: 10.1111/cas.2001.92.issue-8 )
                : 869-873
                Affiliations
                [ 1 ]Department of Surgery II, Nagoya City University Medical School, 1 Kawasumi, Mizuho‐cho, Mizuho‐ku, Nagoya 467‐8601
                [ 2 ]Department of Cancer Biology, Dana‐Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA
                [ 3 ]Department of Adult Oncology, Dana‐Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA
                Author notes
                [*] [* ] To whom requests for reprints should be addressed. E‐mail: hisasaki@ 123456med.nagoya-cu.jp
                Article
                CAE869
                10.1111/j.1349-7006.2001.tb01174.x
                5926835
                11509119
                bec35f60-8129-4bc7-9ae1-1874cbe5e63a
                History
                Page count
                References: 20, Pages: 5
                Categories
                Article
                Custom metadata
                2.0
                August 2001
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.6.9 mode:remove_FC converted:04.11.2015

                periostin,rt‐pcr,lung cancer,prognosis
                periostin, rt‐pcr, lung cancer, prognosis

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