Abstract LB-69: Targeting CK2 with small molecule CX-4945 modulates NF-kappaB, TP53 and cell survival in head and neck squamous cell carcinoma

Author(s):  
Vishnu Kannabiran ◽  
Jay Friedman ◽  
Hai Lu ◽  
Kenna Anderes ◽  
Zhong Chen ◽  
...  
PLoS ONE ◽  
2013 ◽  
Vol 8 (9) ◽  
pp. e73656 ◽  
Author(s):  
Bin Yan ◽  
Huai Li ◽  
Xinping Yang ◽  
Jiaofang Shao ◽  
Minyoung Jang ◽  
...  

Cancers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3759
Author(s):  
Jih-Chin Lee ◽  
Alexander T.H. Wu ◽  
Jia-Hong Chen ◽  
Wen-Yen Huang ◽  
Bashir Lawal ◽  
...  

Despite advancements in diagnostic and standard treatment modalities, including surgery, radiotherapy, and chemotherapy, overall survival rates of advanced-stage head and neck squamous cell carcinoma (HNSCC) patients have remained stagnant for over three decades. Failure of these treatment modalities, coupled with post-therapy complications, underscores the need for alternative interventions and an in-depth understanding of the complex signaling networks involved in developing treatment resistance. Using bioinformatics tools, we identified an increased expression of c-Met, STAT3, and CD44 corresponding to a poor prognosis and malignant phenotype of HNSCC. Subsequently, we showed that tumorsphere-derived exosomes promoted cisplatin (CDDP) resistance and colony and tumorsphere formation in parental HNSCC cells, accompanied by an increased level of oncogenic/immune evasive markers, namely, c-Met, STAT3, CD44, and PD-L1. We then evaluated the therapeutic potential of a new small molecule, HNC0014. The molecular docking analysis suggested strong interactions between HNC0014 and oncogenic molecules; c-Met, STAT3, CD44, and PD-L1. Subsequently, we demonstrated that HNC0014 treatment suppressed HNSCC tumorigenic and expression of stemness markers; HNC0014 also reduced cancer-associated fibroblast (CAF) transformation by Exosp- and CAF-induced tumorigenic properties. HNC0014 treatment alone suppressed tumor growth in a cisplatin-resistant (SAS tumorspheres) mouse xenograft model and with higher inhibitory efficacy when combined with CDDP. More importantly, HNC0014 treatment significantly delayed tumor growth in a syngeneic mouse HNSCC model, elicited an antitumor immune profile, and reduced the total c-Met, STAT3, and their phosphorylated forms, PD-L1 and CD44, contents in serum exosomes. Collectively, our findings provide supports for HNC0014 as a multi-targeted immunotherapeutic lead compound for further development.


2021 ◽  
Author(s):  
Yan Wang ◽  
Peicheng Liu ◽  
Ziwei Zhang ◽  
Jiulong Wang ◽  
Zhigang Cheng ◽  
...  

Background: Recurrent locally advanced or metastatic head and neck squamous cell carcinoma (HNSCC) is associated with dismal prognosis because of its highly invasive behavior and resistance to conventional intensive chemotherapy. The identification of effective markers for early diagnosis and prognosis is important for reducing mortality and ensuring that therapy for HNSCC is effective. Chaperonin-containing TCP-1 3 (CCT3) folds cancer-related proteins to control carcinogenesis. The prognostic value and growth association of CCT3 and HNSCC remains unknown. Methods: The GEO, Oncomine and UALCAN databases were used to examine CCT3 expression in HNSCC. A few clinical HNSCC samples with normal tissues were used to detect CCT3 expression by using immunohistochemistry method. The TCGA-HNSC dataset was used to evaluate the association between expression of CCT3 and prognosis. The molecular mechanism was investigated with gene set enrichment analysis (GSEA). CCK-8 and wound healing assays were used to detect cell growth and invasion of HNSCC, respectively. Results: CCT3 expression was significantly upregulated in HNSCC in both mRNA and protein levels. In addition, upregulated CCT3 expression was associated with various clinicopathological parameters. High expression of CCT3 was significantly correlated with inferior survival of HNSCC patients. Knockdown of CCT3 significantly inhibited cell growth and invasion of HNSCC cell lines. GSEA analysis indicated that CCT3 was closely correlated with tumor-related signaling pathways and HNSCC cell survival. Conclusion: Our findings suggest that CCT3 is a biomarker of poor prognosis and related to the process of HNSCC.


Oncotarget ◽  
2016 ◽  
Vol 7 (18) ◽  
pp. 26307-26330 ◽  
Author(s):  
Uddalak Bharadwaj ◽  
T. Kris Eckols ◽  
Xuejun Xu ◽  
Moses M. Kasembeli ◽  
Yunyun Chen ◽  
...  

Oncotarget ◽  
2019 ◽  
Vol 10 (16) ◽  
pp. 1603-1603
Author(s):  
Uddalak Bharadwaj ◽  
T. Kris Eckols ◽  
Xuejun Xu ◽  
Moses M. Kasembeli ◽  
Yunyun Chen ◽  
...  

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