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  • 1
    In: Digestion, S. Karger AG, Vol. 60, No. 2 ( 1999), p. 117-124
    Abstract: 〈 i 〉 Background: 〈 /i 〉 Carcinoid tumor has been recognized as having a much wider spectrum than was previously thought. Now the term ‘neuroendocrine carcinoma’ (NEC) has been suggested to describe malignant epithelial tumors of neuroendocrine differentiation. Its biological behavior has not been well characterized because of the lack of in vivo models. 〈 i 〉 Materials and Methods: 〈 /i 〉 A metastatic inguinal lymph node from rectal NEC was used for heterotransplantation into nude mice. Histochemical and immunohistochemical stainings were performed in addition to ultrastructural investigations. Hormonal peptides were measured in both xenograft tumor tissue and serum. 〈 i 〉 Results: 〈 /i 〉 We succeeded in heterotransplantation of human rectal NEC into nude mice. To date tumorigenicity has been retained for approximately 38 months. The xenograft tumor was a histopathologically identical tumor. The immunohistochemical expression of the various hormonal peptides in the xenograft was essentially the same as that of the primary rectal tumor. Tissue and serum hormonal peptides in the xenografted tumor were measured. Serum glucagon and serotonin were significantly higher than in control mice. 〈 i 〉 Conclusions: 〈 /i 〉 The expression of various hormonal peptides in NEC may vary depending on the surrounding environment. The establishment of NEC in xenografts provides a model for further study of the biological behavior of NEC, as well as the in vivo effects of chemotherapeutic agents on tumor growth and the release of hormonal peptides.
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 1999
    detail.hit.zdb_id: 1482218-0
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  • 2
    In: Digestion, S. Karger AG, Vol. 57, No. 3 ( 1996), p. 170-173
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
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    Language: English
    Publisher: S. Karger AG
    Publication Date: 1996
    detail.hit.zdb_id: 1482218-0
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  • 3
    Online Resource
    Online Resource
    S. Karger AG ; 2000
    In:  Digestion Vol. 62, No. 4 ( 2000), p. 262-270
    In: Digestion, S. Karger AG, Vol. 62, No. 4 ( 2000), p. 262-270
    Abstract: 〈 i 〉 Background: 〈 /i 〉 Human colorectal neuroendocrine cell carcinoma (NEC) is a rare disease with a poor prognosis. The biological behavior of NEC remains poorly understood. 〈 i 〉 Materials and Methods: 〈 /i 〉 We established two new NEC cell lines from a patient with rectal neuroendocrine carcinoma, NECS-P and NECS-L from the primary tumor and a liver metastasis, respectively. We investigated the biological differences between the two cell lines to study the mechanisms involved in liver metastasis. 〈 i 〉 Results: 〈 /i 〉 There was no difference between NECS-P and NECS-L in the morphological, ultrastructural and immunohistochemical studies. After addition of TGF-β 〈 sub 〉 1 〈 /sub 〉 , the doubling times of NECS-P were increased in a dose-dependent manner relative to untreated cells, whereas TGF-β 〈 sub 〉 1 〈 /sub 〉 had no effect on NECS-L. The attachment and chemotactic response of the two cell lines were not enhanced by TGF-β 〈 sub 〉 1 〈 /sub 〉 . The invasive capacity and the production of matrix metalloproteinase-2 (MMP-2) were significantly increased only in NECS-L following the addition of TGF-β 〈 sub 〉 1 〈 /sub 〉 . When anti-MMP-2 antibody was added to the medium with TGF-β 〈 sub 〉 1 〈 /sub 〉 , NECS-L invasion was inhibited. 〈 i 〉 Conclusion: 〈 /i 〉 It is considered that these differences are important to understand the mechanisms of liver metastasis of NEC.
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2000
    detail.hit.zdb_id: 1482218-0
    Location Call Number Limitation Availability
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  • 4
    In: Digestion, S. Karger AG, Vol. 65, No. 4 ( 2002), p. 200-206
    Abstract: 〈 i 〉 Background: 〈 /i 〉 Somatostatin and its analogues have antitumor effects on foregut and midgut neuroendocrine (NE) tumors, but their effect on hindgut NE tumors is unclear. We examined the effect of the somatostatin analogue, octreotide, on human rectal NE carcinoma. 〈 i 〉 Materials and Methods: 〈 /i 〉 Expression of somatostatin receptor (sst) on NE carcinoma was examined by immunohistochemical staining. Octreotide was added in cell culture medium in order to investigate antiproliferative effect toward NE carcinoma in vitro. Octreotide was administered for 6 weeks to nude mice xenografted with NE carcinoma. We investigated the effect of octreotide on the tumor histologically. The plasma levels of VEGF and bFGF were measured. 〈 i 〉 Results: 〈 /i 〉 The NE carcinoma and endothelial cells expressed sst. Octreotide induced NE carcinoma to apoptosis in vitro and in vivo. Octreotide-treated tumors had a massive necrotic area (62.7 ± 19.3% treated vs. 39.7 ± 20.34% untreated, p 〈 0.05). Microvessels in the treated tumor were decreased (264.0 ± 48.2/mm 〈 sup 〉 2 〈 /sup 〉 treated vs. 341.4 ± 56.6/mm 〈 sup 〉 2 〈 /sup 〉 untreated, p 〈 0.05). The plasma levels of VEGF and bFGF were reduced by octreotide. 〈 i 〉 Conclusions: 〈 /i 〉 Octreotide induces rectal NE carcinoma to apoptosis and inhibits angiogenesis in the tumor. These result in tumor necrosis. Octreotide has an antitumor effect on rectal NE carcinoma.
    Type of Medium: Online Resource
    ISSN: 0012-2823 , 1421-9867
    RVK:
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2002
    detail.hit.zdb_id: 1482218-0
    Location Call Number Limitation Availability
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