Shankar, Varun
(2024)
Deciphering the role of IL-1 signaling as an escape pathway in EGFR-dependent head & neck squamous cell carcinoma (HNSCC): implications for treatment., [Dissertation thesis], Alma Mater Studiorum Università di Bologna.
Dottorato di ricerca in
Oncologia, ematologia e patologia, 36 Ciclo. DOI 10.48676/unibo/amsdottorato/11432.
Documenti full-text disponibili:
|
Documento PDF (English)
- Richiede un lettore di PDF come Xpdf o Adobe Acrobat Reader
Disponibile con Licenza: Salvo eventuali più ampie autorizzazioni dell'autore, la tesi può essere liberamente consultata e può essere effettuato il salvataggio e la stampa di una copia per fini strettamente personali di studio, di ricerca e di insegnamento, con espresso divieto di qualunque utilizzo direttamente o indirettamente commerciale. Ogni altro diritto sul materiale è riservato.
Download (8MB)
|
Abstract
Tumours stemming from the oral cavity, pharynx, larynx, salivary gland, and nasal cavity are collectively placed under Head and Neck Cancer. Overexpressed EGFR accounts for nearly 90% of Head and Neck Cancer. Cetuximab – a chimeric monoclonal antibody was designed to target the extracellular domain III of the EGFR to curtail tumour proliferation. Cetuximab + radiation is the standard therapy for metastatic Head and Neck Cancer, yet, relapse is marked by the aggressive progression of the disease and with a poor survival rate. Patient data acknowledge the role of IL-1 signaling in determining the overall survival in patients. Thus, it becomes imperative to establish the crucial role played by IL-1 cytokines in determining the overall tumorigenesis. In our study, the main intent is to decipher the role played by IL-1 signaling and to overhaul the current treatment strategies with the intention of improving their efficacy. We employed the FaDu tumour cell line and combinatorial drug action by employing both anti-EGFR and anti-IL-1/IL1R1 inhibitors concurrently and found to be more effective in the arrest of overall tumour proliferation compared to mono-therapy (anti-EGFR) alone. We ascertain that combinatorial drug action was found to be effective compared to monotherapy using classical anti-EGFR. Independently, we defined the efficacy of a laboratory-designed anti-IL-1 decoy receptor named human TRAP IL-1 in neutralizing the free IL-1 ligands and the aftermath effects in cells. The results demonstrated the neutralization of IL-1 by TRAP IL-1 besides EGFR boiled down the overall proliferative potential of tumour cells. Summarizing our finding, we verified that IL-1 signaling aids and abets in the proliferation of tumour cells alongside EGFR signaling, thus making both EGFR and IL-1/IL1R1 coupled targets and amending the current treatment strategy with the induction of anti-IL-1/IL1R1 on par with anti-EGFR might increase Progression-Free Survival and Overall Survival in patients.
Abstract
Tumours stemming from the oral cavity, pharynx, larynx, salivary gland, and nasal cavity are collectively placed under Head and Neck Cancer. Overexpressed EGFR accounts for nearly 90% of Head and Neck Cancer. Cetuximab – a chimeric monoclonal antibody was designed to target the extracellular domain III of the EGFR to curtail tumour proliferation. Cetuximab + radiation is the standard therapy for metastatic Head and Neck Cancer, yet, relapse is marked by the aggressive progression of the disease and with a poor survival rate. Patient data acknowledge the role of IL-1 signaling in determining the overall survival in patients. Thus, it becomes imperative to establish the crucial role played by IL-1 cytokines in determining the overall tumorigenesis. In our study, the main intent is to decipher the role played by IL-1 signaling and to overhaul the current treatment strategies with the intention of improving their efficacy. We employed the FaDu tumour cell line and combinatorial drug action by employing both anti-EGFR and anti-IL-1/IL1R1 inhibitors concurrently and found to be more effective in the arrest of overall tumour proliferation compared to mono-therapy (anti-EGFR) alone. We ascertain that combinatorial drug action was found to be effective compared to monotherapy using classical anti-EGFR. Independently, we defined the efficacy of a laboratory-designed anti-IL-1 decoy receptor named human TRAP IL-1 in neutralizing the free IL-1 ligands and the aftermath effects in cells. The results demonstrated the neutralization of IL-1 by TRAP IL-1 besides EGFR boiled down the overall proliferative potential of tumour cells. Summarizing our finding, we verified that IL-1 signaling aids and abets in the proliferation of tumour cells alongside EGFR signaling, thus making both EGFR and IL-1/IL1R1 coupled targets and amending the current treatment strategy with the induction of anti-IL-1/IL1R1 on par with anti-EGFR might increase Progression-Free Survival and Overall Survival in patients.
Tipologia del documento
Tesi di dottorato
Autore
Shankar, Varun
Supervisore
Co-supervisore
Dottorato di ricerca
Ciclo
36
Coordinatore
Settore disciplinare
Settore concorsuale
Parole chiave
Head and Neck Squamous Cell Carcinoma, Cetuximab, Xilonix, Anakinra, Il-1 signaling, EGFR signaling, Overall Survival, Progression Free Survival
URN:NBN
DOI
10.48676/unibo/amsdottorato/11432
Data di discussione
24 Giugno 2024
URI
Altri metadati
Tipologia del documento
Tesi di dottorato
Autore
Shankar, Varun
Supervisore
Co-supervisore
Dottorato di ricerca
Ciclo
36
Coordinatore
Settore disciplinare
Settore concorsuale
Parole chiave
Head and Neck Squamous Cell Carcinoma, Cetuximab, Xilonix, Anakinra, Il-1 signaling, EGFR signaling, Overall Survival, Progression Free Survival
URN:NBN
DOI
10.48676/unibo/amsdottorato/11432
Data di discussione
24 Giugno 2024
URI
Statistica sui download
Gestione del documento: