Papers - Hattori, Yutaka

Restoration of retinoid sensitivity by MDR1 ribozymes in retinoic acid-resistant myeloid leukemic cells

Matsushita Hiromichi, Kizaki Masahiro, Kobayashi Hiroyuki, Ueno Hironori, Muto Akihiro, Takayama Nobuyuki, Awaya Norihiro, Kinjo Kentaro, Hattori Yutaka, Ikeda Yasuo

Blood 91 ( 7 ) 2452-2458 1998.04

Research paper (scientific journal), Joint Work

造血幹細胞への遺伝子導入とその応用

Hattori Yutaka

臨検査 40 ( 8 ) 939-945 1996.08

Research paper (scientific journal), Single Work

Immunohistochemical detection of K-sam protein in stomach cancer

Hattori Yutaka, Itoh Hiroshi, Uchino Shinya, Hosokawa Kouichi, Ochiai Atsushi, Ino Yoshinori, Ishii Hideshi, Sakamoto Hiromi, Yamaguchi Naohito, Yanagihara Kazuyoshi, Hirohashi Setsuo, Sugimura Takashi, Terada Masaaki

Clin Cancer Res 2   1373-1381 1996.08

Research paper (scientific journal), Joint Work

Decreased insulin-like growth factor I receptor expression and function in immortalized african Pygmy T cells

Hattori Yutaka, Vera Carlos Juan, Rivas I Coralia, Bersch Noelle, Bailey C Robert, Geffner E Mitchell, Golde W David

J Clin Endocrinol Metab 81 ( 6 ) 2257-2263 1996

Research paper (scientific journal), Joint Work

Preferential expression of the third immunoglobulin-like domain of K-sam product provides keratinocyte growth factor-dependent growth in carcinoma cell lines.

Ishii H, Hattori Y, Itoh H, Kishi T, Yoshida T, Sakamoto H, Oh H, Yoshida S, Sugimura T, Terada M.

Cancer Research 54   518 - 522 1994

Research paper (scientific journal), Joint Work, Accepted

Preferential alternative splicing in cancer generates a K-sam messenger RNA with higher transforming activity.

Itoh H, Hattori Y, Sakamoto H, Ishii H, Kishi T, Sasaki H, Yoshida T, Kono M, Sugimura T, Terada M.

Cancer Research (AMER ASSOC CANCER RESEARCH)  54 ( 12 ) 3237 - 3241 1994

Research paper (scientific journal), Joint Work, Accepted,  ISSN  0008-5472

　View Summary

K-sam, also designated fibroblast growth factor receptor 2/BEK, was originally cloned from a stomach cancer cell line KATO-III. The gene is amplified and overexpressed preferentially in poorly differentiated types of stomach cancers. The major K-sam transcript in KATO-III cells encodes a receptor protein with a truncated carboxyl terminus and with a high-affinity binding site for keratinocyte growth factor. This truncated type is produced by an alternative splicing mechanism, and in normal tissues, the truncated type is far less prevalent than the untruncated form. The variant K-sam complementary DNA lacks tyrosine 769, which is a putative phospholipase C gamma 1 association site, and showed a higher transforming activity to NIH3T3 cells than the untruncated form, which is identical with the keratinocyte growth factor receptor.

Isolation of the complementary DNA encoding a mouse heparin-binding growth factor receptor with the use of a unique kinase insert sequence.

Katoh O, Hattori Y, Sasaki H, Sakamoto H, Fujimoto K, Fujii T, Sugimura T, Terada M.

Cancer Research (AMER ASSOC CANCER RESEARCH)  53 ( 5 ) 1136 - 1141 1993

Research paper (scientific journal), Joint Work, Accepted,  ISSN  0008-5472

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With the use of reverse transcriptase-polymerase chain reaction techniques focused on a unique kinase insert sequence, the complementary DNA for a mouse tyrosine kinase receptor gene, designated sam3, was isolated from a mouse brain complementary DNA library as a member of the heparin-binding growth factor receptor family or fibroblast growth factor receptor family. The kinase insert region was selected as the probe synthesized by polymerase chain reaction techniques because it composes a unique structure in this receptor family. The sam3 protein, 800 amino acids long, bas high homology to mouse K-sam/bek (67%) and N-sam/flg (63%), which we also cloned as the mouse counterparts of human K-sam/bek and N-sam/flg genes, other members of this family. The sam3 protein also has high homology to human FGFR3 (92%) and chicken cek2 (80%) proteins. The sam3 protein is most likely to be a mouse counterpart of human FGFR3 and chicken cek2 proteins. mRNAs of K-sam/bek, N-sam/flg, and sam3/FGFR3 genes were detected in mouse embryo through some adult tissues. The relative amounts of these mRNAs were different depending on the organs examined. Thus, these gene products may have different biological functions in organ development including the central nervous system.

K-sam-related gene, N-sam, encodes fibroblast growth factor receptor and is expressed in T-lymphocytic tumors.

Hattori Y., Odagiri H, Katoh O, Sakamoto H, Morita T, Shimotohno K, Tobinai K, Sugimura T, Terada M.

Cancer Research (AMER ASSOC CANCER RESEARCH)  52 ( 12 ) 3367 - 3371 1992

Research paper (scientific journal), Joint Work, Accepted,  ISSN  0008-5472

　View Summary

We recently reported the isolation of the K-sam complementary DNA (cDNA), which was amplified preferentially in poorly differentiated types of stomach cancer and codes for one of the heparin-binding growth factor or fibroblast growth factor (FGF) receptor families. The K-sam-related gene, N-sam (NCC-IT-cell-derived sam), was isolated by screening of the cDNA libraries of human immature teratoma cells, NCC-IT. Sequence analysis of the N-sam cDNAs showed that N-sam encodes a human FGF receptor, the FLG protein. N-sam was expressed in lymphocytic leukemia/lymphoma cells, predominantly in the thymic T-cell phenotype. In a T-cell leukemia line, MOLT3, N-sam mRNA expression was markedly enhanced by 12-O-tetradecanoylphorbol-13-acetate treatment and was also up-regulated by basic FGF exposure. These results indicate that N-sam expression is regulated during T-cell ontogeny and modulated by its putative ligand exposure. The results also suggested that interaction between immature T-cell and marrow or thymic interstitial cells might be mediated by N-sam and basic FGF stored in the extracellular matrix of stromal cells.

K-sam gene encodes secreted as well as transmembrane receptor tyrosine kinase.

Katoh M, Hattori Y, Sasaki H, Tanaka M, Sugano K, Yazaki Y, Sugimura T, Terada M.

Proc. Natl. Acad. Sci. USA 89   2960 - 2964 1992

Research paper (scientific journal), Joint Work, Accepted

Expression of the heparin-binding growth factor receptor genes in human megakaryocytic leukemia cells.

Katoh O., Hattori Y, Sato T, Kimura A, Kuramoto A, Sugimura T, Terada M

Biochem. Biophys. Res. Commun. (ACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS)  183 ( 1 ) 83 - 92 1992

Research paper (scientific journal), Joint Work, Accepted,  ISSN  0006-291X

K-sam, an amplified gene in stomach cancer, is a member of the heparin-binding growth factor receptor genes.

Hattori Y, Odagiri H, Nakatani H, Miyagawa K, Naito K, Sakamoto H, Katoh O, Yoshida T, Sugimura T, Terada M.

Proc. Natl. Acad. Sci. USA 87   5983 - 5987 1990

Research paper (scientific journal), Joint Work, Accepted