scholarly journals EXTH-34. COMBINED USE OF THE PAN-IDH MUTANT INHIBITOR AG-881 WITH RADIATION THERAPY SHOWS ADDED BENEFIT IN AN ORTHOTOPIC IDH1 MUTANT GLIOMA MODEL IN VIVO

2017 ◽  
Vol 19 (suppl_6) ◽  
pp. vi79-vi79 ◽  
Author(s):  
Brandon Nicolay ◽  
Rohini Narayanaswamy ◽  
Michael D Amatangelo ◽  
Elia Aguado ◽  
Raj Nagaraja ◽  
...  
2021 ◽  
Author(s):  
Celina Yang ◽  
Kyle Bromma ◽  
Wonmo Sung ◽  
Jan Schuemann ◽  
Devika B. Chithrani

Combined use of chemotherapy and radiation therapy is commonly used in cancer treatment, but the toxic effects on normal tissue are a major limitation. This study assesses the potential to improve radiation therapy when combining gold nanoparticle (GNP) mediated radiation sensitization with chemoradiation compared to chemoradiation alone. Incorporation of GNPs with 2 Gy, 6 MV (megavoltage) radiation resulted in a 19 ± 6% decrease in survival of MDA-MB-231 cells. Monte-Carlo simulations were performed to assess dosimetric differences in the presence of GNPs in radiation. The results show that physics dosimetry represents a small fraction of the observed effect. The survival fraction of the cells exposed to GNPs, cisplatin, and radiation was 0.16 ± 0.007, while cells treated with cisplatin and radiation only was 0.23 ± 0.011. The presence of GNPs resulted in a 30 ± 6% decrease in the survival, having an additive effect. The concentration of the GNPs and free drug used for this study was 0.3 and 435 nM, respectively. These concentrations are relatively lower and achievable in an in vivo setting. Hence, the results of our study would accelerate the incorporation of GNP-mediated chemoradiation into current cancer therapeutic protocols in the near future


2021 ◽  
Author(s):  
Celina Yang ◽  
Kyle Bromma ◽  
Wonmo Sung ◽  
Jan Schuemann ◽  
Devika B. Chithrani

Combined use of chemotherapy and radiation therapy is commonly used in cancer treatment, but the toxic effects on normal tissue are a major limitation. This study assesses the potential to improve radiation therapy when combining gold nanoparticle (GNP) mediated radiation sensitization with chemoradiation compared to chemoradiation alone. Incorporation of GNPs with 2 Gy, 6 MV (megavoltage) radiation resulted in a 19 ± 6% decrease in survival of MDA-MB-231 cells. Monte-Carlo simulations were performed to assess dosimetric differences in the presence of GNPs in radiation. The results show that physics dosimetry represents a small fraction of the observed effect. The survival fraction of the cells exposed to GNPs, cisplatin, and radiation was 0.16 ± 0.007, while cells treated with cisplatin and radiation only was 0.23 ± 0.011. The presence of GNPs resulted in a 30 ± 6% decrease in the survival, having an additive effect. The concentration of the GNPs and free drug used for this study was 0.3 and 435 nM, respectively. These concentrations are relatively lower and achievable in an in vivo setting. Hence, the results of our study would accelerate the incorporation of GNP-mediated chemoradiation into current cancer therapeutic protocols in the near future


10.37206/88 ◽  
2005 ◽  
Author(s):  
Ellen Yorke ◽  
Rodica Alecu ◽  
Li Ding ◽  
Doracy Fontenla ◽  
Andre Kalend ◽  
...  

1996 ◽  
Vol 89 (Supplement) ◽  
pp. S66-S67
Author(s):  
Matthew G. Ewend ◽  
Jeffery Williams ◽  
Betty Tyler ◽  
Richard Anderson ◽  
Khosrow Tabassi ◽  
...  

2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Tong Shen ◽  
Jing-Lin Liu ◽  
Chu-Yi Wang ◽  
Youlutuziayi Rixiati ◽  
Shi Li ◽  
...  

AbstractThe mechanisms and key factors involved in tumor environments for lung metastasis of CRC are still unclear. Here, using clinical samples from lung metastases of CRC patients, we found that intestinal immune network for IgA production was significantly dysregulated in lung metastases of CRC. Single-cell RNA sequencing discovered a subtype of B cells positive for Erbin, one member of the leucine-rich repeat and PDZ domain (LAP) family, was involved in the lung metastases. Erbin deletion in B cells suppressed lung metastasis of CRC in vivo. And, deletion of Erbin in B cells enhanced the killing effects of CD8+ T cells on tumor cells. Mechanistically, Erbin knockout attenuated TGFβ-mediated suppression of migration of CXCR5+ IgA+ cells and STAT6-mediated PD1 expression. Our study uncovered a key role of Erbin in regulating PD1+ IgA+ B cells in lung metastasis of CRC. Targeting Erbin as well as combined use of neutralizing B cells and antibodies neutralizing PD1 suppresses lung metastasis of CRC in mice, suggesting the potential option for treatment of lung metastasis of CRC.


2021 ◽  
Author(s):  
Young‐Suk Choi ◽  
Joonsung Lee ◽  
Han‐Sol Lee ◽  
Jae Eun Song ◽  
Dong‐Hyun Kim ◽  
...  

2007 ◽  
Vol 12 (1) ◽  
pp. 174-186 ◽  
Author(s):  
R.A. Towner ◽  
N. Smith ◽  
S. Doblas ◽  
Y. Tesiram ◽  
P. Garteiser ◽  
...  

2012 ◽  
Vol 135 (2) ◽  
pp. 391-401 ◽  
Author(s):  
Victor C. K. Lo ◽  
Margarete K. Akens ◽  
Sara Moore ◽  
Albert J. M. Yee ◽  
Brian C. Wilson ◽  
...  

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