2 research outputs found
Supplementary Material for: Distinct Involvement of the Sonic Hedgehog Signaling Pathway in Gastric Adenocarcinoma of Fundic Gland Type and Conventional Gastric Adenocarcinoma
<p><b><i>Background/Aims:</i></b> Gastric adenocarcinoma of fundic gland
type (GAFG), which is a rare variant of gastric cancer, is reportedly
associated with both Wnt/β-catenin signaling activation and guanine
nucleotide binding protein, alpha stimulating complex (<i>GNAS</i>) mutations. This study aimed to elucidate potential roles of the Sonic hedgehog (Shh) signaling pathway in GAFG. <b><i>Methods:</i></b>
We performed immunostaining for β-catenin and Shh signal-associated
proteins, including Patched (Ptch), Smoothened (Smo), and
Glioma-associated oncogene-1 (Gli1), and the direct sequencing of <i>GNAS</i>/<i>BRAF</i>/<i>KRAS</i> in 27 GAFGs, and compared them with 30 conventional gastric adenocarcinomas (CGAs). <b><i>Results:</i></b>
GAFGs exhibited significantly lower immunoreactivity scores for Ptch,
Smo, and Gli1 than CGAs. Moreover, while the Ptch score was
significantly lower in the GAFG tumor areas than in the non-neoplastic
areas adjacent to GAFG, the score was significantly higher in the CGA
tumor areas than in the non-neoplastic areas. Similar trends were
observed in the scores for Smo and Gli1. β-Catenin expression and <i>GNAS</i>
mutations were found in 22 (81%) and 8 (30%) of the 27 GAFGs
respectively. Gli1 expression was significantly associated with
mutations in <i>GNAS</i>. <b><i>Conclusion:</i></b> GAFG and CGA
exhibited distinct Ptch, Smo, and Gli1 expression patterns.
Downregulation of the Shh signaling pathway, as well as activation of
the Wnt/β-catenin signaling pathway, may therefore be associated with
tumorigenesis in GAFG.</p
Supplementary Material for: The Effects of All-Trans Retinoic Acid on the Induction of Oral Tolerance in a Murine Model of Bronchial Asthma
<b><i>Background:</i></b> Active suppression induced by regulatory T (Treg) cells is reported to be one of the mechanisms involved in oral tolerance. All-trans retinoic acid (ATRA) has been reported to affect Treg cell differentiation. The present study examined the effects of ATRA on the induction of oral tolerance in a murine model of bronchial asthma. <b><i>Methods:</i></b> BALB/c mice were sensitized to and challenged with ovalbumin (OVA) through feeding followed by OVA challenges. In some study groups ATRA was orally administered concomitantly with OVA feeding either in the presence or absence of the retinoic acid receptor antagonist LE135. Lung CD4<sup>+</sup> T cells were isolated from mice exposed to ATRA and/or OVA, and transferred to control mice. Airway hyperresponsiveness (AHR), cell counts and cytokine levels in bronchoalveolar lavage (BAL) fluid, and lung histology were assessed. <b><i>Results:</i></b> Concomitant administration of ATRA with OVA ameliorated AHR, airway eosinophilia, elevation of cytokines in BAL fluid and goblet cell metaplasia. The proportion of Treg cells in the lungs was increased in mice treated with OVA and ATRA, as compared to those treated with OVA only. Transfer of lung CD4<sup>+</sup> T cells from mice treated with OVA and ATRA induced suppression of AHR and airway inflammation. LE135 completely reversed the effects of ATRA on AHR, airway allergic inflammation and the number of Treg cells in the lungs. <b><i>Conclusion:</i></b> These data suggested that oral administration of ATRA with OVA had the potential to enhance oral tolerance in this murine model of bronchial asthma. These effects were mediated, at least in part, by Treg cell expansion