15 research outputs found

    Immunohistochemical expression of p14 MMTV env protein in feline mammary carcinomas.

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    <p>(A) FMC # 84471. Tubulopapillary FMC PCR-negative and negative for MMTV p14 expression (Immunoperoxidase-DAB, Bar = 100 μm) (B) FMC # 84589. Tubulopapillary FMC PCR-positive, a weak cytoplasmic immunostaining was detected in some neoplastic epitrhelial cells (Immunoperoxidase-DAB, Bar = 100 μm). (C) FMC # 80613. Tubolopapillary FMC, some neoplastic epithelial cells show distict cytoplasmic MMTV p14 labelling (Immunoperoxidase-DAB, Bar = 100 μm). (D) FMC # 86367. Solid FM, a large number of carcinoma cells show cytoplasmic p14 staining, Scattered inflammatory cells associated with neoplastic proliferation resulted MMTV p14-positive (Immunoperoxidase-DAB, Bar = 100 μm).</p

    Determination of phylogentic relationships of Env sequences identified in different hosts.

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    <p>A neighbor-joining phylogenetic tree from nucleotide sequences of env of MMTV viruses. The tree was rooted to HERV-K. The robustness of individual nodes of the tree was determined by using bootstrap analyses of 1,00 replicates.</p

    Multiple nucleotide alignment of the MMTV-like env gene sequences.

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    <p>A) The env sequences from two feline mammary tumors (indicated by their respective number) were aligned with NIH 3T3 (positive control for MMTV), mouse mammary tumor virus from HeJ mice, and HMTV (accession numbers AF228551.1 and AF243039, respectively). B) DNA sequencing, confirming the MMTV sequences. Surprisingly, one of them (Cat 87768) showed a polymorphism (c.7575 A> G), that cause aminoacyl substitution (Thr> Ala).</p

    Loss of c-KIT expression in thyroid cancer cells

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    <div><p>Papillary thyroid carcinoma is the most frequent histologic type of thyroid tumor. Few studies investigated the role of c-KIT expression in thyroid tumors, suggesting a role for this receptor and its ligand in differentiation and growth control of thyroid epithelium and a receptor loss following malignant transformation. We investigated and correlated c-KIT expression levels and two known markers of thyrocytes differentiation, PAX8 and TTF-1, in malignant and benign cytological thyroid samples. Moreover, we performed functional studies on human papillary thyroid carcinoma cell line to associated c-KIT expression to thyrocytes differentiation and tumor proliferation. c-KIT and PAX8 expression resulted higher in benign samples compared to the malignant ones, and the expression levels of these two genes were significantly correlated to each other. We also observed that c-KIT overexpression led to an increase of PAX8 expression level together with a decrease of proliferation. Furthermore, c-KIT overexpressing cells showed a regression of typical morphological features of malignancy. Taken together these results suggest that c-KIT could be involved in the differentiation of thyroid cells and in tumor progression.</p></div
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