Abstract 174: Keratin 8 and 18 knockdown increases cisplatin-induced apoptosis and invasive potential through claudin1/PI3K/NFkB up-regulation in epithelial carcinoma cells
Notice bibliographique
Résumé
Abstract Keratins are epithelial-specific intermediate filament (IF) proteins, which are expressed in a tissue-specific manner. As part of the cytoskeleton, keratins are important for the mechanical stability and integrity of epithelial cells and tissues. Moreover, a number of keratins are involved in intracellular signalling pathways which regulate response to injuries and non-mechanical stresses, cell growth, cell death and cancer progression. Keratins 8 and 18 (K8/18) are typically co-expressed as the primary keratin pair in simple epithelial cells and their expression are maintained during malignant transformation, hence their use as diagnostic marker in tumor pathology. However, in recent years different studies have shown that IF should not be considered only as markers proteins but also as regulators of cancer cell signaling and that they might play an active role in malignant transformation. In the present study, we addressed the question as to whether K8/18 expression affects tumor fate and behaviour. Our results show that K8/18 stable knockdown using shRNA increases cisplatin sensitivity in three different epithelial cancer cell lines. Indeed, western blot analysis of caspases activation and flow cytometry analysis of AnnexinV/PI staining show that K8/18 knockdown sensitizes cells to cisplatin-induce apoptosis. Increased FasL expression and FasR membrane targeting suggest that apoptosis is enhanced via the death receptor pathway. Moreover, using in vitro wound healing and transwell invasion assays, we observed that K8/18-knockdowned cancer cells display an increased cellular motility and invasion. Interestingly, we observed that these cells present higher PIP3 levels in the plasma membrane as determined by both fluorescence microscopy and flow cytometry analysis. Consequently, the K8/18-shRNA clones show PI3K/Akt/PKC/NFkB pathways hyperactivation and increased MMP-9 expression. Furthermore, these processes are shown to be partially regulated by the tight junction's protein claudin-1, which is highly increased in K8/18-shRNA clones. To our knowledge, these results represent the first indication that K8/18 can influence the phenotype of epithelial cancer cells. Knockdown of K8/18 increases cisplatin sensitivity and invasive potential of epithelial cancer cell lines through the regulation of different cell signaling pathways, involving claudin-1 dependent PI3K activation and NFkB transcription activity. These results support the hypothesis that modulation of K8/18 expression plays an active role in cancer progression. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 174. doi:1538-7445.AM2012-174
Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.
Comment cette classification a été obtenuedéplier
Prédiction distillée sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.
Scores Codex et Gemma par catégorie
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,001 | 0,000 |
| Méta-épidémiologie (sens strict) | 0,000 | 0,000 |
| Méta-épidémiologie (sens large) | 0,000 | 0,000 |
| Bibliométrie | 0,000 | 0,000 |
| Études des sciences et des technologies | 0,000 | 0,000 |
| Communication savante | 0,000 | 0,000 |
| Science ouverte | 0,000 | 0,000 |
| Intégrité de la recherche | 0,000 | 0,000 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,000 | 0,000 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».