scholarly journals Metabolic reprogramming by folate restriction leads to a less aggressive cancer phenotype

Author(s):  
Z. Ashkavand ◽  
C. O'Flanagan ◽  
M. Hennig ◽  
X. Du ◽  
S. D. Hursting ◽  
...  
2017 ◽  
Vol 15 (2) ◽  
pp. 189-200 ◽  
Author(s):  
Zahra Ashkavand ◽  
Ciara O'Flanagan ◽  
Mirko Hennig ◽  
Xiuxia Du ◽  
Stephen D. Hursting ◽  
...  

2014 ◽  
Author(s):  
Yosuke Togashi ◽  
Hiroki Sakamoto ◽  
Hidetoshi Hayashi ◽  
Masato Terashima ◽  
Marco A. de Velasco ◽  
...  

2014 ◽  
Vol 13 (1) ◽  
pp. 126 ◽  
Author(s):  
Yosuke Togashi ◽  
Hiroki Sakamoto ◽  
Hidetoshi Hayashi ◽  
Masato Terashima ◽  
Marco A de Velasco ◽  
...  

Author(s):  
Hamda Al-Thawadi ◽  
Lina Ghabreau ◽  
Tahar Aboulkassim ◽  
Amber Yasmeen ◽  
Semir Vranic ◽  
...  

Epstein–Barr virus (EBV) has been recently shown to be co-present with high-risk human papillomaviruses (HPVs) in human cervical cancer; thus, these oncoviruses play an important role in the initiation and/or progression of this cancer. Accordingly, our group has recently viewed the presence and genotyping distribution of high-risk HPVs in cervical cancer in Syrian women; our data pointed out that HPVs are present in 95.45% of our samples. Herein, we aim to explore the co-prevalence of EBV and high-risk HPVs in 44 cervical cancer tissues from Syrian women using polymerase chain reaction (PCR), immunohistochemistry (IHC) and tissue microarray (TMA) analyses. We found that EBV and high-risk HPVs are co-present in 15/44 (34%) of the samples. Additionally, we report that the co-expression of LMP1 and E6 genes of EBV and high-risk HPVs, respectively, is associated with poorly differentiated squamous cell carcinomas phenotype; this is accompanied by a strong and diffused Id-1 overexpression, which is an important regulator of cell invasion and metastasis. These data imply that EBV and HPVs are co-present in cervical cancer in the Middle East area including Syria and their co-presence is associated with a more aggressive cancer phenotype. Future investigations are needed to elucidate the exact role of EBV and HPVs cooperation in cervical carcinogenesis.


2020 ◽  
Vol 6 (26) ◽  
pp. eaba3231
Author(s):  
Emilia M. Pinto ◽  
Bonald C. Figueiredo ◽  
Wenan Chen ◽  
Henrique C.R. Galvao ◽  
Maria Nirvana Formiga ◽  
...  

Cancer risk is highly variable in carriers of the common TP53-R337H founder allele, possibly due to the influence of modifier genes. Whole-genome sequencing identified a variant in the tumor suppressor XAF1 (E134*/Glu134Ter/rs146752602) in a subset of R337H carriers. Haplotype-defining variants were verified in 203 patients with cancer, 582 relatives, and 42,438 newborns. The compound mutant haplotype was enriched in patients with cancer, conferring risk for sarcoma (P = 0.003) and subsequent malignancies (P = 0.006). Functional analyses demonstrated that wild-type XAF1 enhances transactivation of wild-type and hypomorphic TP53 variants, whereas XAF1-E134* is markedly attenuated in this activity. We propose that cosegregation of XAF1-E134* and TP53-R337H mutations leads to a more aggressive cancer phenotype than TP53-R337H alone, with implications for genetic counseling and clinical management of hypomorphic TP53 mutant carriers.


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