IL1 Pathway in HPV-Negative HNSCC Cells Is an Indicator of Radioresistance After Photon and Carbon Ion Irradiation Without Functional Involvement
Treatment of locally advanced HPV-negative head and neck squamous cell carcinoma (HNSCC) with photon radiation is the standard of care but shows only moderate success. Alterations in response toward DNA DSB repair, apoptosis, and senescence are underlying determinants of radioresistance in the tu...
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Format: | Artikel |
Sprache: | Englisch |
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Philipps-Universität Marburg
2022
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Zusammenfassung: | Treatment of locally advanced HPV-negative head and neck squamous cell
carcinoma (HNSCC) with photon radiation is the standard of care but shows only moderate
success. Alterations in response toward DNA DSB repair, apoptosis, and senescence are
underlying determinants of radioresistance in the tumor cells. Recently, senescence and the
associated secretory phenotype (SASP) came into the focus of research and raised the
need to identify the tumor-promoting molecular mechanisms of the SASP. The aim of this
project was to unravel more of this process and to understand the impact of the IL1
pathway, which plays a major role in SASP. The studies were performed for photon and
12C-ion irradiation, which strongly vary in their effect on radioresistance.
panel of five HPV-negative HNSCC cell lines was treated with
photon and 12C-ion irradiation and examined for clonogenic survival, DNA DSB repair, and
senescence. SASP and IL1 gene expressions were determined by RNA sequencing and
activation of the IL1 pathway by ELISA. A functional impact of IL1A and IL1B was
examined by specific siRNA knockdown.
Cell killing and residual DSBs were higher after 12C-ion than after photon
irradiation. 12C-ion induced more senescence with a significant correlation with cell
survival. The impact on radioresistance appears to be less than after photon irradiation.
The expression of SASP-related genes and the IL1 pathway are strongly induced by both
types of irradiation and correlate with radioresistance and senescence, especially IL1A
and IL1B which exhibit excellent associations. Surprisingly, knockdown of IL1A and IL1B
revealed that the IL1 pathway is functionally not involved in radioresistance, DSB repair, or
induction of senescence.
IL1A and IL1B are excellent indicators of cellular radioresistance and
senescence in HNSCC cells without functional involvement in these processes. Clearly
more research is needed to understand the molecular mechanisms of senescence and
SASP and its impact on radioresistance. |
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Beschreibung: | Gefördert durch den Open-Access-Publikationsfonds der UB Marburg. |
Umfang: | 13 Seiten |
DOI: | 10.3389/fonc.2022.878675 |