Volume 57, Issue S8 pp. 108-109
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Ectopic expression of c-kit in small-cell lung cancer

Toyoaki Hida

Toyoaki Hida

Department of Internal Medicine, Aichi Cancer Center, Nagaya 464, Japan

Laboratory of Chemotherapy, Aichi Cancer Center, Nagaya 464, Japan

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Ryuzo Ueda

Ryuzo Ueda

Laboratory of Chemotherapy, Aichi Cancer Center, Nagaya 464, Japan

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Yoshitaka Sekido

Yoshitaka Sekido

Laboratory of Immunology, Aichi Cancer Center, Nagaya 464, Japan

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Kenji Hibi

Kenji Hibi

Laboratory of Immunology, Aichi Cancer Center, Nagaya 464, Japan

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Ryohei Matsuda

Ryohei Matsuda

Department of Internal Medicine, Aichi Cancer Center, Nagaya 464, Japan

Laboratory of Chemotherapy, Aichi Cancer Center, Nagaya 464, Japan

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Yutaka Ariyoshi

Yutaka Ariyoshi

Department of Internal Medicine, Aichi Cancer Center, Nagaya 464, Japan

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Takahiko Sugiura

Takahiko Sugiura

Department of Internal Medicine, Aichi Cancer Center, Nagaya 464, Japan

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Takashi Takahash

Corresponding Author

Takashi Takahash

Laboratory of Chemotherapy, Aichi Cancer Center, Nagaya 464, Japan

Laboratory of Chemotherapy, Aichi Cancer Center, Nagaya 464, JapanSearch for more papers by this author
Toshitade Takahashi

Toshitade Takahashi

Laboratory of Immunology, Aichi Cancer Center, Nagaya 464, Japan

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First published: 1994
Citations: 23

Abstract

Accumulating evidence suggests that c-kit plays an important role in the regulation of growth of at least 3 lineages of stem cells, while only very limited data are available on the development of human solid tumors. Our recent studies have shown that c-kit transcripts are expressed in a very restricted sub-set of human solid tumors such as small-cell lung cancer (SCLC). We have also conducted an immunohistological study on in situ localization of the c-Kit protein in various human solid tumors as well as in corresponding fetal and adult normal tissues. No c-kit expression was detected in normal bronchial epithelial cells or pneumocytex in lung parenchyma of human fetal and adult specimens, indicating that the c-kit protein is aberrantly expressed in lung-cancer cells. We also found that significant chemotactic response as well as moderate in vitro cell growth occurred in SCLC cell lines upon addition of recombinant human stem-cell factor.

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