Introduction of gene polymorphisms in aldehyde dehydrogenase 2
Function of aldehyde dehydrogenase 2 in human beings
The aldehyde dehydrogenases play a key role in the metabolism of toxic aldehydes. Some are produced in human bodies, such as 4-hydroxy-2-nonenal (4-HNE) and malondialdehyde (MDA), while others were obtained from the environment, like formaldehyde, acrolein, and ethyl.1,2 As a member of the ALDH superfamily, ALDH2 is the most sensitive isoform to irreversible inactivation and is also the most sensitive to inactivation by toxics, such as 4-HNE.1 This enzyme could metabolize acetaldehyde (ACH) to acetate irreversibly in a redox reaction (Fig. 1).3 Disturbances in the expression of ALDH2 will dampen its metabolic capacity and result in accumulation of ACH consequently. Based on its electrophilic feature, ACH could bind with biomolecules such as proteins or DNA and destroy cell integrity, which contributes to the development of various human diseases,4 such as endocrine disorders, cardiovascular diseases, pulmonary diseases, oral cancers, gastrointestinal cancers, Fanconi anemia, and dermatitis.5–7
ALDH2 gene and polymorphisms
ALDH2 is a polypeptide consisting of 517 amino acids, principally expressed in the liver but also in other organs, such as heart, kidney, muscle, and brain.8 Its coding gene is located on chromosome 12 (12q24.2), which is 44 kilobases in length and comprises 13 exons.9 After translation, the expressed protein is transported to the mitochondrial matrix to participate in dehydrogenase, esterase and reductase reactions in liver and fat tissues particularly. Studies of the human genome have shown 19 kinds of functional ALDH genes in total, with a wide range of expression and substrate specificities, among which the ALDH2 gene has the highest expression and exclusively harbors existence of genetic polymorphisms.1
As it encodes a key enzyme for alcohol metabolism, ALDH2 also has an important functional single nucleotide polymorphism (SNP), the rs671-Glu504Lys variant, which has significantly reduced activity compared to the wild type.10 The rs671 variant exists in 30–45% of East Asians (Chinese, Japanese, and Korean) and 8% of the world’s population.11,12 The incidence of this mutation in China is as high as 37–59%.13–16 Nowadays, the rs671SNP locus at exon 12 is of special concern in worldwide research. According to sequencing detection,17 a G→A point mutation is prone to occur at exon 12, causing the original glutamic acid (Glu) to be replaced by lysine (Lys), whose mutation is named ALDH2Glu504Lys (SNPrs671).
ALDH2rs671 SNPs are composed of three genotypes: GA, AA and GG. GA is a heterozygous mutation, also named as ALDH2*1/*2 (Glu/Lys). AA is a homozygous mutation, also known as ALDH2*2/*2 (Lys/Lys). GG is the normal allele, without mutation (Fig. 2). The majority of studies on these genotypes have confirmed that the GA genotype has 10–20% of the enzyme activity compared wild type, while the AA genotype loses more than 96% of the enzymatic activity. As a result, individuals with GA or AA mutations could show up to 6 or 19 times greater ACH concentrations, respectively, as compared with wild type after alcohol intake.18
Distribution of ALDH2 alleles in different populations
The genotype frequencies of the ALDH2 gene polymorphisms vary among different races. The rare ALDH2*2 allele has been observed in Caucasians, Africans and Southeast Asians but it is widely present in East Asians.19,20 There is a report of this mutation being found in about 560 million people of East Asian descent and reducing enzymatic activity by approximately 60% to 80% in ALDH2*1/*2 heterozygotes.19 Among East Asians, the ALDH2 allele frequencies are diverse among Japanese, Korean, and Chinese. In China, the ALDH2*2 gene frequency in some Chinese aboriginal populations (e.g., Korean, Uighur, Zhuang and Olunchun) is lower compared to the Chinese Han population. In the Chinese Han population, the ALDH2*2 allele frequency is 17% to 29%, the proportion of individuals with ALDH2*1/*2 heterozygotes is 36% to 44%, and the proportion of individuals with ALDH2*2/*2 homozygotes is 7% to 8%.21,22
Related liver diseases
Alcoholic liver disease
Alcoholic liver disease (ALD) is a direct outcome of chronic ethanol consumption and is considered as an important health problem worldwide. ALD encompasses a broad spectrum of liver injuries, including steatosis, fibrosis, cirrhosis, and alcoholic hepatitis.23 The incidence of ALD has been increasing yearly because of the rapid boom in alcohol consumption in many developing countries over the past decade.24 The prevalence of ALD in China, the USA, Europe, and Japan is 4.5%, 6.2% ,6%, and 1.56–2.34%, respectively.24–27 There are about 260 million people occasionally, habitually and excessively drinking, and appropriately 2.5 million people die from ALD each year.28 Hence, ALD pathogenesis and therapy have always been the focus of national researchers.
The ALDH2 Glu504lys polymorphism is tied closely to occurrence and development of ALD in related individuals,29 though its polymorphism does not contribute to alcohol dependence in the Turkish population.30 Regardless of homozygous AA or heterozygous GA status, both guarantee elevated ACH level after alcohol drinking. A single-center study from the Fifth Medical Centre of the General Hospital of the Chinese People’s Liberation Army reported that only 2.3% of ALD patients have the ALDH2*2 allele, compared with14.5% of the proportion of healthy controls (281 and 535 controls; odds ratio [OR] of 0.13 and 95% confidence interval [CI] of 0.07–0.24).31 In Korea, Lee et al.32 found that the ALDH2*1 allele is associated with a higher frequency of alcoholic cirrhosis (p=0.001). Likewise, a meta-analysis of 12 studies found that people with the ALDH2*1 allele are more likely to go on to develop alcoholic liver cirrhosis compared with those with either the ALDH2*1/*2 or ALDH2*2/*2 genotype.33 Based on the activity of the enzyme after gene mutation, ALDH2*2/*2 should have produced a poor protective effect of ethanol; however, it brings some body information, such as facial flushing, reminding those with ALDH2*2/*2 to be alert to alcohol intake and usually leading to little excessive ethanol consumption.34 On the contrary, without the gene reminder, those with ALDH2*1 are not aware of consuming excessive alcohol.
The protection from the ALDH2 Glu504lys polymorphism has also been verified by Liu’s team,35 whose result demonstrated that individuals carrying this polymorphism are protected from alcohol drinking, with a 4-fold decrease in risk. Ma et al.36 and Li et al.16 also provided further evidence that the mutation and “alcohol flush” are not harmless in this Asian population. In other words, the ALDH2 gene mutation is a protective factor in the alcohol-drinking population in East Asia, while it is weaker in European and African populations.34 In fact, the Eastern culture encourages or challenges people to drink more alcohol in social activities, and sometimes people with flushing may not be able to escape or reject such alcoholism.
Aerobic glycolysis is involved in alcohol metabolism, which could be inhibited by a known factor: corticosterone. As is shown in the animal experiment of Gao’s team,37 a higher level of serum corticosterone is detected in ethanol-fed Aldh2(−/−) mice, compared to the wild type mice. Gao’s team37 also found that acute alcohol drinking in humans was related to elevated plasma glucocorticoid levels in human subjects, with higher levels in those with inactive ALDH2 than active ALDH2. To conclude, the progress of aerobic glycolysis is impaired by ethanol, especially in those with ALDH2*2. Meanwhile, they succeeded in restored concanavalin A-mediated hepatitis via blockade of corticosterone. Therefore, aerobic glycolysis-related signaling pathways may be a key factor. Interestingly, the authors found that glucose metabolism in T cells could be disrupted by ACH through inhibition of the aerobic glycolysis-related signal pathways. In addition, weakened autophagy is involved and compromised lysosomal activity will lead to abnormal stacking of ethanol or acetaldehyde by-product including protein or DNA adducts. Guo et al.38 reported that observations both in vivo and in vitro are in favor of a beneficial role of ALDH2 in alcohol intake-facilitated fatty liver and inflammation through autophagy regulation (Table 116,30–37).
Table 1Recent clinical studies on the relationship between the ALDH2 polymorphism and ALD
| Year | Conclusion | Reference |
|---|
| 2001 | The ALDH2*2 gene protects against the development of alcoholism. | 32 |
| 2012 | Strong protective effect of the ALDH2 504lys (*2) allele against alcoholism and alcohol-induced medical diseases in Asians. | 16 |
| 2015 | The absence of the ALDH2*2 allele in both alcoholics and controls suggests that this polymorphism does not contribute to alcohol dependence in the Turkish population. | 30 |
| 2015 | ALDH2 plays a beneficial role in ameliorating chronic alcohol intake-induced hepatic steatosis and inflammation, through regulation of autophagy. | 37 |
| 2016 | People with the ALDH2*1 allele are more likely to go on to develop alcoholic liver cirrhosis compared with those with the ALDH2*1/*2 or ALDH2*2/*2 genotype. | 33 |
| 2016 | Polymorphisms in ALDH2 exerted significant indirect effects on hepatocellular carcinoma risk, mediated through alcohol drinking. | 35 |
| 2016 | The ALDH2 Glu504Lys polymorphism and ‘alcohol flush’ are not harmless in the study’s Asian population. | 36 |
| 2017 | Individuals who carry at least one copy drink typically less and are protected against heavy alcohol use and alcohol use disorders. | 34 |
| 2018 | Patients with the ALDH2 504lys variant were less associated with ALD compared to those with ALDH2 504glu. | 31 |
| 2019 | ALDH2 deficiency is associated with elevated acetaldehyde and glucocorticoids post-alcohol consumption, thereby inhibiting T cell activation and hepatitis. | 37 |
The traditional hypothesized pathway is through oxidative stress. ALDH2 dramatically attenuates hepatic oxidative stress induced by chronic alcohol intake and favors a role of oxidative stress in ethanol- and ALDH2-elicited hepatic responses, by restoring autophagy and reopening autophagy flux. Additional ethanol consumption will increase the production of NADH/NAD+, and reactive oxygen species (ROS) in the mitochondrial electron transport chain. Then, ROS is able to activate nuclear factor-kappa B (NF-κB) and its downstream proinflammatory signal, and correspondingly aggravate inflammation and hepatocyte damage.39–41 Moreover, Zhong et al.42 selected mitochondrial ALDH2 as a promising therapeutic target for ALD. They said that it accelerates aldehyde clearance and reverses hepatic steatosis and apoptosis in mice. Therefore, artificial modulation of ALDH2 expression may be a potential therapeutic intervention for alcoholism and ALD in the future.43,44
As mentioned above, variants in ALDH2 decrease the rate of ACH conversion to acetate because it blocks its ability to remove ACH and results in a strong aversive reaction. Therefore, if we can find a medium to intervene this mechanism and develop a blocker, we will alleviate this effect. It is also suggested that physicians should pay attention to explore the potential immunosuppressive therapy in alcoholics.
Non-alcoholic fatty liver disease
It has become more and more accepted that non-alcoholic fatty liver disease (NAFLD) stands for not just a single type of liver disease but the hepatic manifestation of complicated metabolic dysfunctions. NAFLD covers a wide range of liver pathologies, including steatosis, steatohepatitis, fibrosis/cirrhosis and liver failure.14,45 Nowadays, NAFLD has become the leading cause of chronic liver diseases on earth and its global prevalence is appropriately 25%.46–49 Prevalence rates of NAFLD were estimated to be 22.4%, 24.13%, 23.71%, 25%, 31% and 32% in China, the USA, Europe, Japan, the Middle East, and South America, respectively.14,24,50,51 In the USA, NAFLD is estimated to be the most common cause of chronic liver disease, affecting between 80 and 100 million individuals, among whom nearly 25% progress to non-alcoholic steatohepatitis.14 A recent report of data from the National Health and Nutrition Examination Survey ranging from 1988 to 2010 indicated that modest alcohol consumption (7–21 g/day) is associated with decreased mortality among patients with NAFLD.52 In contrast to the studies of 58,927 patients with NAFLD in Korea, even moderate drinkers (10–29.9 g/day) exhibited an increased tendency to progress to fibrosis compared with non-drinkers.53 Whether consuming moderate alcohol could be a lifestyle intervention in the treatment requires further investigation.
In China and East Asia, genome-wide association studies found that ALDH2 rs671 is a susceptible gene locus for obesity and significantly associated with increased body mass index and visceral fat deposition.10,11 A control study reported that a significant accumulation of the 4-HNE protein adduct and a significant up-regulation of ALDH2 protein expression are found in the two groups of non-alcoholic steatohepatitis patients, suggesting that ALDH2 plays a role in combating non-alcoholic steatohepatitis oxidative stress. We have reason to speculate that ALDH2 gene mutation will reduce the oxidative stress protection response of liver recovery in non-alcoholic steatohepatitis patients. On the contrary, Alda-1, as an activator of ALDH2, suppresses PINK1/PARKIN-mediated mitophagy and its usage in apoE-mice has led to improvement in the degree of arteriosclerosis and hepatic steatosis, indicating that activation of ALDH2 can improve NAFLD on the condition of mitochondrial injury caused by vinyl chloride.54 Alda-1 protects against liver damage under these conditions via increasing clearance of aldehydes and preserving mitochondrial respiratory function.
In the field of biomedicine, researchers have found that inhibition of ALDH2 enhances the ACH-mediated hepatocyte sterol regulatory element binding protein-1 (SREB-1) pathway activity and promotes triglyceride (TG) deposition in the liver. A cohort study55 conducted by Japanese researchers followed 341 patients who never or seldom drank or drank less for 4–6 years and found that the incidence of NAFLD is higher in carriers of the mutant gene ALDH2*2 than in non-carriers. Carriers of ALDH2*2 with elevated γ-glutamyl transpeptidase (GGT) levels (>25.5 IU/L) have a significantly increased risk of NAFLD. A recent Japanese study investigated the association of ALDH2rs671 genotype with liver disease in 1,768 alcohol-dependent Japanese men. They found that the ineffective ALDH2 Glu/Lys genotype increases the ratio or regression coefficient of age- and alcohol-adjusted fatty liver, ketonuria and serum high-density lipoprotein cholesterol (HDL-C) level, and reduces liver cirrhosis and serum TG level. Through logistic regression analysis, Chinese scientists also found that the GGT level in carriers of the GA/AA type is significantly higher than that of the GG type, suggesting that carriers of the GA/AA type are more prone to suffer liver cell damage and more severe fatty changes than carriers of the GG type. Nevertheless, another animal study suggested that ALDH2-deficient individuals may be resistant to steatosis and blood alanine aminotransferase (ALT) elevation but be more prone to liver inflammation and fibrosis following alcohol consumption.15 Furthermore, a human experiment showed that the prevalence of elevated ALT level increases with the accumulation of components of metabolic syndrome and that the correlation between active ALDH2 and elevated ALT level is sensitive.56 Their logistic regression analysis also revealed that body mass index, TG level, and ALDH2 genotype are associated with ALT elevation. This result coincides with the findings of the genome-wide association studies.
To conclude, the relationship between ALDH2 and the NAFLD disease spectrum has begun to enter the laboratory stage but it needs a large number of research studies to clarify the connection.
Viral hepatitis
Although the global incidence of viral hepatitis, hepatitis B virus (HBV) infection mainly, is going down, it continues to play an important role in developing countries.57 There are approximately 257 million people with chronic HBV infection globally, including 68% in Africa and the Western Pacific, according to a World Health Organization report.58 In China, chronic hepatitis B (CHB) and chronic hepatitis C (CHC) affect 90 million and 10 million people, respectively. In developed countries such as the USA, Japan, and the European Union, the prevalence of HBV is much lower (0.71–1.17%), but the prevalence of hepatitis C virus (HCV) (1.10–1.56%) is higher than in China (HBV: 6.52%; HCV: 0.72%). In 2016, the Global Health Sector Strategy on viral hepatitis called for elimination of viral hepatitis as a major public health threat by 2030.59 However, unlike other liver diseases, the relationship between viral hepatitis and ALDH2 remains unclear.
HCV infection is an important cause of chronic liver disease, with nearly 71 million chronically infected people worldwide.57 HCV and alcohol intake are both risk factors for accelerated fibrosis progression,60 and alcohol use in the setting of HCV infection is correlated with increased rates of fibrosis progression.61 Based on previous studies,62,63 the correlation between ALDH2 and HCV could be explained by the two following aspects: enhanced virus replication and immunity suppression.
For one thing, the metabolite ACH could help to activate the expression of miR-122 and miR-34a, both able to stimulate HCV replication.64 Correspondingly, a large number of virus products brought about by strong virus replication will promote hepatocellular apoptosis. Apoptosis has a secondary amplification effect on the viral lethality in the liver, which not only delays virus clearance but also aggravates liver cell damage. And, then, Kupffer cells and hepatic stellate cells (HSC) are driven by interleukins to aggregate and participate in the phagocytosis and clearance of apoptotic bodies.62 This process will accelerate the inflammatory responses and fibrogenesis in the liver. Meanwhile, ACH could increase the activity of protein phosphatase 2A (PP2A).65 PP2A could reduce methylation of signal transducer and activator of transcription (STAT)-1 and formation of the protein inhibitor of the activated STAT-1 PIAS-1-STAT-1 complex.64 Ultimately, the damage will enhance destruction of STAT-1 caused by HCV, thereby increasing the apoptosis (Fig. 3).
For another, some scientists have claimed that impairment of immunity is a probable cause. Ethanol exposure enhances the inhibitory effect of HCV on innate immunity, thereby activating the spread of the virus in the liver and eventually leading to impaired adaptive immunity.63 The expression of interferon-stimulated genes (commonly referred to as ISGs) compromises over 300 antiviral molecules that synergistically exert innate immunity and are under control of the catalysis of retinol and retinoic acid biogenesis.65 Interestingly, the toxicity of these two substances can be suppressed by ALDH metabolism. It means that inhibition of ALDH will hinder the body’s antiviral ability through the ISGs pathway. Therefore, one of the molecular mechanisms for the synergism between HCV and alcohol abuse in liver disease progression is hepatocyte metabolism involving ethanol-retinol metabolic competition.66
In addition, activated T cells can be combined with other immune cells to form a positive feedback effect, being aroused by various cellular factors in turn, in a bid to stir up inflammation and inhibiting further liver damage. Gao et al.37 discovered the phenomena that alcohol-fed Aldh2−/− mice were less sensitive to concanavalin A-induced T cell hepatitis than wild type mice. Their further study suggested that ACH directly restrained cytokine production in T cells by means of the inhibition of aerobic glycolysis or stimulation of corticosterone release, leading to the occurrence of suppressed T cell hepatitis in ethanol-fed Aldh2−/− mice. What is more, there is a certain correlation between the HBV epidemic area and the distribution of ALDH2 gene-defect areas in East Asia.67 Almost all patients with ALDH2 mutation genotypes are linked with HBV infection.68 Among patients with chronic HBV, homozygous carriers of the ALDH2*2 mutant gene have a significantly increased risk of developing liver cirrhosis.
Generally speaking, there is an optimistic link between ALDH2 and HCV, and alcohol is undoubtedly a factor that aggravates the development of HCV disease and may also be a break-through point in the design of research experiments.
Hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is the sixth most common cancer and the third leading cause of cancer mortality in the world.69 In China, HCC has emerged as one of the top three malignant tumors, according to rankings by prevalence and mortality.70,71 The prevalence rates of HCC were reportedly 0.03%, 0.01%, <0.01%, and <0.01% among the general population in China, the USA, Europe, and Japan, respectively.25 Meanwhile, HCC cases are increasing rapidly in China,69 which accounts for approximately 90% of all cases of primary liver cancer.72 Therefore, scientists have been endeavoring to explore the relationship between ALDH2 gene mutation and HCC (Table 235,73–79).
Table 2Recent clinical studies on the relationship between the ALDH2 polymorphism and HCC
| Author | Year | Conclusion | Reference |
|---|
| Liu et al. | 2016 | Polymorphisms in ALDH2 had significant indirect effects on HCC risk, mediated through alcohol drinking. | 35 |
| Hou et al. | 2017 | Inhibiting aggressive behavior both in vitro and in mice by forcing the expression of ALDH2 in HCC cells. | 73 |
| Ye et al. | 2018 | The mutant genotypes of ALDH2 may be protective factors for HCC susceptibility in Guangxi Province, China. | 74 |
| Chien et al. | 2016 | GG genotype of ALDH2 rs671 was an HCC risk predictor in cirrhotic chronic hepatitis B patients. | 75 |
| Seo et al. | 2019 | ALDH2 deficiency is associated with an increased risk of alcohol-related HCC development from fibrosis in human patients and in mice. | 76 |
| Chen et al. | 2020 | ALDH2 rs671 polymorphisms are not associated with HCC susceptibility in East Asians. | 77 |
| Huang et al. | 2019 | HCC patients carrying a defective allele of ALDH2 had a favorable postoperative outcome. | 78 |
| Jin et al. | 2015 | ALDH 2 plays a role of tumor suppressor by maintaining the stability of genome in the liver, and the common human ALDH 2 variant would become an important risk factor for hepatocarcinogenesis. | 79 |
Generally, HBV infection and ALD are two major liver diseases with HCC developing tendency.60 Hou et al.73 inhibited aggressive behavior in vitro and in mice by forcing the expression of ALDH2 in HCC cells. Recently, Liu et al.35 explored the association between ALDH2 polymorphisms and the risk of HCC among CHB patients, and their result showed that ALDH2 polymorphisms has nothing to do with HCC but does protect against developing HCC through habitual alcohol drinking, which was reported in another research study as well.74 Similarly, based on an analysis of 4,155 hepatitis B surface antigen seropositive participants, there is a distinct relationship between an increased risk of HCC in the HBV-positive cirrhosis population and ALDH2 gene polymorphisms.75 Recently, a study involving both mice and human patients showed that ALDH2 gene deficiency correlates well with a higher risk for advancement of alcohol related-fibrosis to HCC.76
A meta-analysis conducted by Chen et al.77 found that the ALDH2 rs671 polymorphism is not associated with HCC susceptibility in East Asians, and this is similar to the conclusion from Liu et al.35 Interestingly, Huang et al.78 found that the ALDH2 polymorphisms had a certain impact on resolution of HCC in patients. The result showed that HCC patients with a defective allele of ALDH2 have a promising postoperative outcome, after Kaplan-Meier analysis and univariate followed by multivariate Cox proportional hazard analysis indicated that the GG genotype is an independent clinical predictor for shorter time-to-distant metastasis (adjusted p=0.019) and shorter overall survival (adjusted p=0.001). Although the ALDH2*2 mutation itself does not lead to liver cancer directly, it will reduce ALDH2 protein levels and liver enzyme, which eventually is related to the accumulation of ACH in the blood and carcinogenic mutations. Likely, the results of animal experiments show that the mouse ALDH2 (E487K) mutation significantly promotes the occurrence and development of mouse liver cancer.79
Unfortunately, despite a series of strong evidence supporting ethanol as an environmental risk factor for HCC, the exact pathways by which alcohol causes HCC are still under exploration. ACH has been shown to affect DNA replication and repair mechanisms. After chronic alcohol exposure, Aldh2-deficient animals produce a large amount of harmful oxidized mitochondrial DNA via extracellular vesicles, which can be delivered into neighbor HCC cells and subsequently activate multiple oncogenic pathways, to promote HCC development (Fig. 4).76 What is more, consuming a large amount of ethanol induces microsomal ethanol metabolism by cytochrome P4502E1 (known as CYP2E1) and leads to additional production of acetaldehyde, as well as an increase in free radicals that can result in cell death, DNA damage, and even production of other carcinogenic substances.80,81 Other hypothesized pathways have included the transactivator protein X that is encoded by HBV and remolded to the extracellular matrix through hypoxia-inducible factor-1α (HIF-1α) target genes and the lysyl oxidase (HIF-1α/LOX) pathway to promote HCC metastasis.82 The ALDH2-acetaldehyde-redox-AMP-activated protein kinase (AMPK) axis participates in the regulation of ACH levels, which is activated by ALDH2. Therefore, identifying ALDH2 expression levels in HCC might be a useful biomarker for determining prognosis and developing targeted therapies that are urgently needed to treat patients with HCC.
In addition, human liver cancer tissue test results show that ALDH2*2 protein is extremely unstable in human liver, and the low expression of ALDH2 protein has a certain correlation with the formation of liver cancer. The Journal of Hepatology also reports that a deficiency in the ALDH2 gene expression is associated with an increased risk of HCC in patients with hepatitis B cirrhosis who overtake alcohol. Both in vivo and in vitro studies have found that liver cells from ALDH2-deficient mice can produce a large amount of harmful oxidized mitochondrial DNA,32 which is transferred to adjacent liver cells through extracellular vesicles and can activate multiple carcinogenic pathways involving ACH (JNK , STAT3, BCL-2, and TAZ) to promote the occurrence of alcohol-related HCC.73 ALDH2 could also affect metabolism by regulating the ALDH2-acetaldehyde-redox-AMPK axis,83 because AMPK can direct lipid metabolism to regulate tumor cell growth and survival. Actually, in proteomics studies, among the proteins related to metabolism and liver function, ALDH2 does not have the highest expression level of enzymes, compared to ALDH1, ALDH4 and ALDH9A, according to the characteristics of the metabolic subgroup;84 however, we cannot look down upon the role of ALDH2 in HCC. Zahid et al.85 reported transcriptional suppression of alcohol metabolism regulators, and demonstrated that ALDH2, downstream of the mTOR signal, is partly responsible for triggering oncogenic transformation of hepatocytes, resulting in disease onset and progression in HCC in silico.
In summary, ALDH2 is a potential risk factor for HCC. However, the clinical correlation between ALDH2 gene polymorphism and the occurrence and development of liver cancer remains to be further studied.