2016
DOI: 10.1002/mc.22459
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Transcriptome profiling in oral cavity and esophagus tissues from (S)‐N′‐nitrosonornicotine‐treated rats reveals candidate genes involved in human oral cavity and esophageal carcinogenesis

Abstract: Recently, we have shown that (S)-N′-Nitrosonornicotine [(S)-NNN], the major form of NNN in tobacco products, is a potent oral cavity and esophageal carcinogen in rats. To determine the early molecular alterations induced by (S)-NNN in the oral and esophageal mucosa, we administered the carcinogen to rats in the drinking water for 10 weeks and global gene expression alterations were analyzed by RNA sequencing. At a false discovery rate p-value < 0.05 and fold-change ≥ 2, we found alterations in the level of 39 … Show more

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Cited by 6 publications
(6 citation statements)
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References 52 publications
(60 reference statements)
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“…13 Very recently, AIRE expression was reported in human and mouse keratinocytes and in tumors originating in stratified and pseudostratified epithelia, as head and neck squamous carcinomas. 16,17 Thus, the shared feature of promiscuous expression of some genes by mTECs and cancer cells 18,19 raises the possibility that analogous mechanisms of transcriptional regulation operate in both cell types and that AIRE, as part of or a consequence of such mechanisms, is ectopically activated in some solid human tumors.…”
Section: Introductionmentioning
confidence: 99%
“…13 Very recently, AIRE expression was reported in human and mouse keratinocytes and in tumors originating in stratified and pseudostratified epithelia, as head and neck squamous carcinomas. 16,17 Thus, the shared feature of promiscuous expression of some genes by mTECs and cancer cells 18,19 raises the possibility that analogous mechanisms of transcriptional regulation operate in both cell types and that AIRE, as part of or a consequence of such mechanisms, is ectopically activated in some solid human tumors.…”
Section: Introductionmentioning
confidence: 99%
“…Only two patients with stage II or stage III ESCCs that did not have preceding neoadjuvant therapies were enrolled in this study; accordingly, we predicted that the number of enrolled patients might not be enough to meet a statistical significance. Instead, we enrolled patients with stage II or III OSCCs in the study, because they likely had similar TMEs to ESCCs, and they shared the same pathologic diagnoses and carcinogenic pathways as described above [ 26 , 27 , 28 ]. Besides, patients with stage II or III OSCCs are usually treated by surgery alone, without any preceding neoadjuvant therapies.…”
Section: Discussionmentioning
confidence: 99%
“…This suggests the difficulty of enrolling a sufficient number of patients with advanced ESCCs that have been solely treated by surgery as a control group. Instead, we enrolled patients with oral squamous cell carcinoma (OSCC) in this study; OSCC is considered to be comparable to ESCC, because they share similar pathologic diagnoses, squamous cell carcinoma, carcinogenic pathways (such as alcohol drinking and smoking), and molecular features [ 26 , 27 , 28 , 29 ]. Additionally, ESCC is usually treated by neoadjuvant CRT or chemotherapy followed by surgery, as described above, whereas OSCC is rarely treated with neoadjuvant chemotherapy or CRT before surgery.…”
Section: Introductionmentioning
confidence: 99%
“…FETUB, a liver-derived plasma protein, has recently been reported to influence glucose metabolism (36). FETUB copy number amplification in human esophageal cancer, head and neck squamous cell carcinoma was at least 10–23% (37). FETUB was associated with decreased lung function in patients with chronic obstructive pulmonary disease (COPD), and predicted the occurrence of acute exacerbation or frequent acute exacerbation (38).…”
Section: Discussionmentioning
confidence: 99%