Abstract:The aldehyde dehydrogenase 2 point mutation (ALDH2*2) is a common frequent human gene variant, especially in East Asians. However, the expression and mechanism of action of ALDH2 in HNSC remain unknown. The present study explored the clinical significance and immune characteristics of ALDH2 in HNSC. The receiver operating characteristic curve was analysed to assess the diagnostic value of ALDH2 expression. ALDH2 expression in normal tissues and HNSC tissues was evaluated by IHC, and we also analysed ALDH2 gene… Show more
“… 49 And the ALDH2 gene is associated with the JAK-STAT signaling pathway. 50 According to the above studies, the results on the relationship between the risk of DM and HTN and the ALDH2 rs671 polymorphisms used as a predictor for the risk of T2DM still need more evidence with different sample sizes, regions, and ethnicities. Moreover, little is known about the link between ALDH2 gene polymorphisms and the risk of DM in HTN patients, and identification of susceptibility ALDH2 genes and other risk factors would be helpful for the prevention and treatment of DM in HTN patients.…”
Background
Aldehyde dehydrogenase 2 (
ALDH2
) polymorphisms have been extensively studied in patients with hypertension (HTN) and diabetes mellitus (DM) in recent years. However, it is unclear whether
ALDH2
polymorphisms are correlated with the risk of developing DM in patients with HTN. This study was designed to examine the association between
ALDH2
single nucleotide polymorphism (SNP) rs671 and the risks of DM in patients with HTN.
Methods
This study retrospectively analyzed the patients with HTN who were treated in Meizhou People’s Hospital from August 2016 to December 2020, 788 HTN patients with DM as case patients, and 1632 HTN patients without DM history as controls.
ALDH2
polymorphisms were analyzed using a polymerase chain reaction (PCR)-gene chip. Differences in
ALDH2
genotypes between subjects and controls were compared. To analyze the relationship between
ALDH2
genotype and DM risk, multiple logistic regression analysis was performed after adjusting for gender, age, smoking history, and drinking history.
Results
The proportion of the G/A plus A/A genotype was significantly higher in patients with DM than in controls (52.8% vs 48.2%,
P
=0.033). DM patients with G/A genotype had lower LDL-C (
P
<0.017) than those with G/G genotype. The results of logistic regression analysis indicated that the G/A genotype increased the risk of DM in HTN patients, with an adjusted odds ratio (OR) of 1.209 (95% confidence interval (CI) 1.010–1.446) (
P
=0.038), whereas the G/A plus A/A genotype in the dominant model increased the risk of DM significantly, with an adjusted OR of 1.203 (95% CI 1.013–1.428) (
P
=0.035).
Conclusion
ALDH2
A allele (G/A + A/A genotype) increased the risk of DM in patients with HTN.
“… 49 And the ALDH2 gene is associated with the JAK-STAT signaling pathway. 50 According to the above studies, the results on the relationship between the risk of DM and HTN and the ALDH2 rs671 polymorphisms used as a predictor for the risk of T2DM still need more evidence with different sample sizes, regions, and ethnicities. Moreover, little is known about the link between ALDH2 gene polymorphisms and the risk of DM in HTN patients, and identification of susceptibility ALDH2 genes and other risk factors would be helpful for the prevention and treatment of DM in HTN patients.…”
Background
Aldehyde dehydrogenase 2 (
ALDH2
) polymorphisms have been extensively studied in patients with hypertension (HTN) and diabetes mellitus (DM) in recent years. However, it is unclear whether
ALDH2
polymorphisms are correlated with the risk of developing DM in patients with HTN. This study was designed to examine the association between
ALDH2
single nucleotide polymorphism (SNP) rs671 and the risks of DM in patients with HTN.
Methods
This study retrospectively analyzed the patients with HTN who were treated in Meizhou People’s Hospital from August 2016 to December 2020, 788 HTN patients with DM as case patients, and 1632 HTN patients without DM history as controls.
ALDH2
polymorphisms were analyzed using a polymerase chain reaction (PCR)-gene chip. Differences in
ALDH2
genotypes between subjects and controls were compared. To analyze the relationship between
ALDH2
genotype and DM risk, multiple logistic regression analysis was performed after adjusting for gender, age, smoking history, and drinking history.
Results
The proportion of the G/A plus A/A genotype was significantly higher in patients with DM than in controls (52.8% vs 48.2%,
P
=0.033). DM patients with G/A genotype had lower LDL-C (
P
<0.017) than those with G/G genotype. The results of logistic regression analysis indicated that the G/A genotype increased the risk of DM in HTN patients, with an adjusted odds ratio (OR) of 1.209 (95% confidence interval (CI) 1.010–1.446) (
P
=0.038), whereas the G/A plus A/A genotype in the dominant model increased the risk of DM significantly, with an adjusted OR of 1.203 (95% CI 1.013–1.428) (
P
=0.035).
Conclusion
ALDH2
A allele (G/A + A/A genotype) increased the risk of DM in patients with HTN.
“…Identification of key biomarkers to assess tumor prognosis raises implications for early tumor diagnosis, treatment regimen selection, and cancer prevention ( Economopoulou et al, 2019 ). The prognosis of patients with head and neck cancer is related to many factors, such as age, smoking, gender, TNM stage, stage, drug sensitivity, immune cell infiltration, etc ( Zhang et al, 2020 ; Zhang et al, 2021 ; Yao et al, 2022 ). In this work, we got 47 ferroptosis-related genes to obtain a correlation with the prognosis of head and neck cancer patients from the FerrDb database.…”
Ferroptosis is that under the action of ferrous iron or ester oxygenase, unsaturated fatty acids highly expressed on the cell membrane are catalyzed to undergo lipid peroxidation, thereby inducing cell death. In this study, we used ferroptosis marker genes to identify 3 stable molecular subtypes (C1, C2, C3) with distinct prognostic, mutational, and immune signatures by consensus clustering; TP53, CDKN2A, etc. Have higher mutation frequencies in the three subtypes. C3 has a better prognosis, while the C1 subtype has a worse prognosis. WGCNA is used to identify molecular subtype-related gene modules.After filting, we obtained a total of 540 genes related to the module feature vector (correlation>0.7).We performed univariate COX regression analysis on these genes, and identified a total of 97 genes (p < 0.05) that had a greater impact on prognosis, including 8 ‘‘Risk” and 89 ‘‘Protective” genes. After using lasso regression, we identified 8 genes (ZNF566, ZNF541, TMEM150C, PPAN, PGLYRP4, ENDOU, RPL23 and MALSU1) as ferroptosis-related genes affecting prognosis. The ferroptosis prognosis-related risk score (FPRS) was calculated for each sample in TCGA-HNSC dataset. The results showed that FPRS was negatively correlated with prognosis.The activated pathways in the PFRS-high group mainly include immune-related pathways and invasion-related pathways. We assessed the extent of immune cell infiltration in patients in our TCGA-HNSC cohort by using the expression levels of gene markers in immune cells. The FPRS-high group had a higher level of immune cell infiltration. We found that the expression of immune checkpoints was significantly up-regulated in the FPRS-low group and the FPRS-high group had a higher probability of immune escape and a lower probability of benefiting from immunotherapy. In this work, we constructed a scoring Ferroptosis-related prognostic model that can well reflect risk and positive factors for prognosis in patients with head and neck squamous cell carcinoma. It can be used to guide individualized adjuvant therapy and chemotherapy for patients with head and neck cancer. Therefore, it has a good survival prediction ability and provides an important reference for clinical treatment.
“… 63 Moreover, ALDH2 is linked to autophagy regulation in some diseases, and it was speculated that autophagy is one of the mechanisms that ALDH2 uses to regulate tumor occurrence and development. 64 , 65 In addition, ALDH2 indirectly regulates the immune system due to its role in aldehydes metabolism and acetaldehyde adducts, 66 , 67 and it may also be one of the mechanisms by which ALDH2 is involved in tumor development.…”
Colorectal cancer (CRC) is a cancer that occurs in the colon or rectum and can occur in any part of the colon, with the rectum and sigmoid colon being the most common. 1 According to the latest global cancer statistics, the incidence (19.5 people per 100,000 people) and mortality (9.0 people per 100,000 people) of CRC rank third and second, respectively. 2 In China, the incidence of CRC increased rapidly, and
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