HBE cells were purchased from the Xiangya Hospital Cell Bank (Central South University, Changsha, China). The base growth medium was Dulbecco's modified Eagle's medium (DMEM; HyClone; Cytiva). This was supplemented with fetal bovine serum(FBS; 10%; Sigma-Aldrich; Merck KGaA) as well as penicillin/streptomycin (100 U/ml penicillin/100 µg/ml streptomycin). HBE cells had been stored in liquid nitrogen, before being thawed rapidly in a 37°C water bath. The cells were then dispensed into a 75 cm² culture flask; the flask was then stored in an incubator at 5% CO₂. The growth medium was changed the following day.

The original CSE solution was prepared using an aqueous medium; when smoke from burnt cigarettes passed through a sealed jar containing water, the toxic compounds contained in the smoke were collected in the solvent. During the experiment, the same cigarette brand was used and the original CSE solution was prepared on the day of the experiment. HBE cells were cultured at 37°C for 24 h with DMEM. Following this, the base medium was replaced with growth medium containing the final CSE. Flasks received growth media with CSE concentrations of 2.5, 5, 7.5, 10, 12.5 or 15%. The original CSE solution was prepared with DMEM on the day of the experiment, with the final concentration determined by spectrophotometry. At 24, 48, and 72 h post-CSE treatment, an immunofluorescence assay was performed on the cells to detect benzopyrene-DNA adducts. The optimal time-point and CSE concentration for benzopyrene-DNA adduct formation was recorded. These parameters were then used for subsequent experiments. With reference to the literature and previous experiments (26,27), the concentrations used for EGCG treatment were 0, 5, 10, 20 and 40 µM. A gene microarray technique was used to detect the differential miRNA expression profiles of the treated HBE cells.

A CCK-8 (MedChemExpress) assay was used to detect the survival rate of HBE cells. Cells were plated in 96-well plates at a density of 8×10⁴ cells/ml before CSE and EGCG treatments were performed. These cells were then cultured at 37°C in an incubator at 5% CO₂ for 24, 48 and 72 h. The treated medium was replaced with 100 µl of the CCK-8 solution (CCK-8: PBS, 1:9). The plates were then wrapped in tin foil before being incubated at 37°C for a further 2 h. The absorbance was then measured at 450 nm on an enzyme-labeling instrument. Each experiment was repeated 3 times.

HBE cells were cultured on cell slides in 24-well plates. Following the treatment regimens, an immunofluorescence assay was performed. A specific BPDE-DNA adduct mouse monoclonal antibody (1:100; cat. no. sc-52625; Santa Cruz Biotechnology, Inc.) was used to detect DNA lesions in the HBE cells. The slide was incubated in a wet box at 4°C overnight. The cells were stained with DAPI (10 µg/ml; cat. no. D1306; Thermo Fisher Scientific, Inc.) at room temperature for 10 min. The slides were then sealed with an anti-fluorescence quenching agent (containing 90% glycerin; Thermo Fisher Scientific, Inc.) before images were captured under a fluorescence microscope (1:4 and 1:400).

The treated HBE cells were washed with PBS. Cells were lysed with TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.). Total RNA was extracted using a Mini miRNA extraction kit (cat. no. 217004; Qiagen China Co., Ltd.). RNA integrity was assessed using RNA denaturation electrophoresis (Bioanalyzer 2100; Agilent). miRNA microarray hybridization experiments and data collection were performed by the Wuhan Google Biotechnology Co., Ltd. A miRNA microarray hybridization chip (cat. no. G4474A; Agilent Technologies, Inc.) was scanned using an Agilent Microarray Scanner. The featured extraction software version 10.7.1.1 (Agilent Scan Control software) was used to collect and analyze data. The fold change of differentially screened miRNA was at least two-fold compared with the control group. Functional changes to miRNA expression levels following EGCG treatment were determined by comparative analysis. Furthermore, bioinformatics technology was used to predict the target genes and signaling pathways affected by EGCG treatment. The miRNA target gene prediction softwares, miRDB (http://mirdb.org/miRDB), Diana microT v3.0 (http://diana.cslab.ece.ntua.gr/microT) and TargetScan 3.0 (http://www.targetscan.org/), were used to predict the target genes of the selected miRNA. Targeted signaling pathways were predicted by the signaling pathway analysis software 'Ingenuity Pathway Analysis' (http://www.ingenuity.com). The most important miRNA was further validated in tissue samples by fluorescence in situ hybridization. The experiment was carried out according to the instructions of a FAM-Labeled Probe Detection kit (Wuhan Servicebio Technology Co., Ltd.). The sequence of the gene-specific oligonucleotide probe was 5′-FAM-ACA GGC ACC CCA CTC CAC AGA-FAM-3′ for miRNA-7114-5p. The sections were dewaxed with xylene for 15 min. For RNA retrieval, the sections were placed into boiling water for 15 min and cooled naturally. Subsequently, the sections were digested with protease K (20 µg/ml; Wuhan Servicebio Technology Co., Ltd.) at 37°C for 30 min. Following incubation with pre-hybridization solution at 37°C for 1 h, the sections were treated with probe miRNA-7214-5p hybridization solution (8 ng/µl) and placed in an incubator at 37°C overnight. Tissue sections were stained with DAPI (10 µg/ml), incubated in darkness for 8 min, and sealed with anti-fluorescence quenching agent. The images were collected under a fluorescence microscope.

Non-small cell lung cancer specimens and adjacent tissues, atypical hyperplasia, and chronic inflammatory tissues were collected. Tissue samples were collected from 30 patients, including 19 males and 11 females, aged 37 to 68 years. This research protocol was approved by the Medical Ethics Committee of Xiangya Hospital of Central South University (approval no. 201703133), and paraffin-embedded tissue samples were selected from the specimen bank of the Department of Pathology of Xiangya Hospital. These samples were preserved and paraffin-embossed after surgical treatment at the Department of Thoracic Surgery of Xiangya Hospital from May 2018 to October 2019. All patients provided written informed consent before surgery. Retrospective investigation of clinical data revealed that all patients with non-small cell lung cancer had a lung mass or nodule which was found by enhanced CT examination, and were confirmed as non-small cell lung cancer by postoperative pathological diagnosis. Para-carcinoma tissue was defined as lung tissue removed from the margin of lung cancer tissue of more than 20 mm. The patients with atypical hyperplasia or pulmonary inflammation were those who had a lung mass or pulmonary nodule suspected diagnosis such as lung cancer (possibly lung cancer) by enhanced CT scan before operation and confirmed atypical hyperplasia or pulmonary inflammation by pathological diagnosis after surgical resection. Continuous 4-µm thick tissue sections were sliced. Immunohistochemistry was used to detect protein expression in different lung tissues. For immunohistochemical protein detection, xylene was used to dewax the paraffin sections. For antigen retrieval, the sections were placed into a sodium citrate buffer (pH 6.0) and heated in a microwave for 2 min before being placed in a water bath (98°C), for a further 20 min. The expression levels of NF-κB (1:200), transforming growth factor (TGF)-β (1:200) and CYP1A1 (1:200) proteins were detected by their respective specific rabbit-antibodies: product no. ADI-KAS-TF110-D (Enzo Life Sciences, Inc.); and cat. nos. MBS462142 and MBS127670; MyBioSource, Inc.). The slides were incubated in a wet box at 4°C overnight. Tissue known to express the target protein was used as a positive control, while tissue known to have an absence of the protein was used as a negative control. DAB staining (at room temperature for 15 min) was used to assess the results. A scoring system from 0-3 was devised; unstained cells scored 0, mild yellow staining scored 1, strong yellow staining scored 2 and brown staining scored 3. The percentage of cells positively stained was also scored; <5% was 0 points, 5-25% was 1 point, 26-50% was 2 points, and >50% was 3 points. These scores were then multiplied to provide an overall grading; a score of 0-1 was negative (−), 2-3 was weakly positive (+), 4-6 was positive (++) and a score of 6-9 was strongly positive (+++).

Female Sprague Dawley (SD) rats, aged 6-8 weeks and weighing 180-200 g, were purchased from the Department of Experimental Animals (Central South University, Changsha, China). A total of 60 rats were randomly divided into three groups. Animals were caged in groups of five. The rats were kept at room temperature (24±2°C), 50% humidity and in a 12-h light/dark cycle with adequate food and water supply. The control and cigarette smoke (CS) treatment groups were administered normal drinking water, while the EGCG group received water supplemented with EGCG (0.3%) (13,42). The EGCG solution was prepared and changed daily. Following 2 weeks of drinking the solution, the rats inhaled CS. All rats in the CS +/− EGCG treatment groups were exposed to 90 min of CS a day, 5 days a week (43-45). The rats were treated in a transparent glass cage. A total of 10 cigarettes were lit at a time. In each round of exposure, the rats were treated with passive smoke for 15 min, the sealed cover of the cage was then opened and the rats were allowed to breathe 'clean' air for 15 min. During the next round of exposure, rats were passively exposed to smoke for 90 min, with close attention paid to the activity of the rats during this period. Following this exposure, smoking treatment was immediately discontinued if there was evidence of breathing difficulties (rapid breathing, salivation, and cyanosis). On the 4, 8, 12 and 16th weekend following the introduction of CS, 5 rats from each treatment group were sacrificed. Rats received an intraperitoneal injection of a chloral hydrate solution (300 mg/kg), before being sacrificed under anesthesia. In brief, after weighing the rats with an electronic balance, the required 10% chloral hydrate solution was calculated. The anesthetic solution was extracted with a syringe and injected into the abdominal cavity of the rats. The rats quickly lost consciousness after the injection, and none of the rats exhibited signs of peritonitis, pain or discomfort. After the breathing of the rat became slow and weak and it did not respond to stimulation, the rat was sacrificed by exsanguination from the carotid artery under the conditions of unconsciousness and painlessness. All of the animals were treated humanely and in compliance with the Animal Welfare Act of America. The experiment was approved (approval no. 201703133) by the Ethics Department of Xiangya Hospital, Central South University (Changsha, China).

Tissue from each lung of the treated rats was obtained, completely immersed in 4% paraformaldehyde at room temperature, fixed for 24 h. This was then transferred to a 0.2% sodium azide solution at room temperature, and tissue continued to be fixed for 24 h before being embedded in paraffin. Each lobe was sectioned in 5 consecutive slices at a thickness of 5 µm. Each section was stained with 0.5% hematoxylin for 10 min and 0.5% eosin for 3 min and analysis was performed independently by two pathologists.

Prepared rat lung sections were dewaxed in xylene and then alcohol. These sections were then placed in a 0.1 mol/l citric acid buffer solution (pH=6) and microwaved for 20 min to retrieve antigens (microwave oven PM100). The tissue was blocked using 10% goat serum (Beijing Zhongshan Jinqiao Biotechnology, Inc.) at room temperature for 1 h in a wet box. Staining for benzopyrene-DNA adducts in the rat lung samples was performed using an anti-BPDE-adduct mouse monoclonal antibody (1:100) for 1 h at room temperature. The sections were then rinsed and incubated with a secondary goat anti-mouse antibody (1:200; LS-C56298; LifeSpan BioSciences, Inc.) for 60 min at room temperature. Positive and negative samples, where benzopyrene-DNA adducts were present or absent, were used as controls. After the experiment was completed, the glass slides were sealed with an anti-fluorescence quenching agent. The benzopyrene-DNA adducts were observed and images were captured using a fluorescence microscope, before the average optical density was assessed by ImageJ software v1.8.0 (National Institutes of Health).

Total RNA of rat lung tissue was extracted according to the Direct-zol™ RNA MiniPrep Quick Protocol (Zymo Research Corp). RNA was reverse transcribed to cDNA using the High Capacity cDNA Reverse Transcription Kit (cat. no. 4368813; Applied Biosystems; Thermo Fisher Scientific, Inc.). A total of 50-µl reaction volumes, containing 500 ng of sample RNA, were prepared for cDNA amplification. Using a Bio-Rad MyCycler™, the reaction was carried out at 25°C for 10 min, 37°C for 120 min and held at 4°C upon completion. The GAPDH gene was amplified as a positive control, an RT negative sample was produced using the same reaction mixture without reverse transcriptase. The cDNA products were diluted at 1:10 for use in qPCR. qPCR was performed using an ABI Quantstudio™ 3 Real-Time PCR System, with SYBR Green Master Mix (Bio-Rad Laboratories, Inc.). Primers were synthesized by Shanghai Biotechnology Co., Ltd. and were as follows: NF-κB forward, 5′-GGC TTC TAT GAG GCT GAA CTC TGC-3′ and reverse, 5′-CTT GCT CCA GGT CTC GCT TCT TC-3′; CYP1A1 forward, 5′-CAG GAC AGG AGG CTG GAC GAG-3′ and reverse, 5′-ACC AGG TAC ATG AGG CTC CAA GAG-3′; GAPDH forward, 5′-GAC ATG CCG CCT GGA GAA AC-3′ and reverse, 5′-AGC CCA GGA TGC CCT TTA GT-3′. The q-PCR reactions were carried out at 94°C initial denaturation for 2 min; 40 of cycles at 94°C denaturation for 15 sec, 60°C annealing, elongation and fluorescence was read for 1 min; and 60°C final extension for 4 min. All data were analyzed using the 2^−ΔΔCq method (46).

Rat lung tissue was collected to determine the level of NF-κB and CYP1A1 protein expression. Lung tissue was washed twice with cold TBS and crushed in a 1.5-ml homogenate tube, before being placed on ice and suspended in RIPA buffer (cat. no. G2002; Wuhan Servicebio Technology Co., Ltd.) with protein inhibitor. The mixture was placed in an ice-bath for 30 min, centrifuged 13,000 × g at 4°C for 15 min, before the supernatant was removed in a clean tube and stored at -80°C. To perform the western blot analysis, 16 µl of sample containing 150 µg of protein was loaded along with 1.6 µl of 10X SDS buffer and 4 µl of SDS buffer per well of a 10% SDS-PAGE gel, then electrophoresis was performed at 80 V for 100 min. Electrophoresis was stopped and the protein on the gel was transferred to a nitrocellulose membrane at 60 V for 120 min. The membrane was then blocked with 5% fat-free milk for 1 h at room temperature. The membrane was then incubated with mouse specific NF-κB (1:1,000; cat. no. GB11142; Wuhan Servicebio Technology Co., Ltd.) and CYP1A1 (1:1,000; cat. no. sc-101828; Santa Cruz Biotechnology, Inc.) antibodies overnight at 4°C. Next, the membrane was washed three times with TBS-T (0.1% Tween-20) buffer for 10 min. The membrane was then incubated with a goat anti-rat secondary antibody (1:3,000; GB23302; Wuhan Servicebio Technology Co., Ltd.) for 2 h at room temperature, before the washing step was repeated. Finally, the blot was developed using a prepared A (luminol) and B (hydrogen peroxide), 1:1 reagent mix and incubated at room temperature for 5 min, before images were captured using a ChemiDoc™ XRS+ system with Image Lab™ Software V6.0 (Bio-Rad Laboratories, Inc.).

The data are presented as the mean ± SD of three repeats. SPSS 24.0 (IBM Corp.) statistical software was used to analyze the data. A paired Student's t-test was used for comparison between two groups. One-way analysis of variance (ANOVA) was used for comparison between multiple groups. The pairwise comparisons among the multiple groups were conducted using Tukey's post hoc test. All statistics were bilateral. The test level was set as α=0.05, and P<0.05 was considered to indicate a statistically significant difference. GraphPad Prism v. 6 (GraphPad Software, Inc.) was used to create all the graphs.

After CSE treatment, two types of damage occurred in the HBE cells. Acute toxicity was associated with a decreased survival of HBE cells. When the CSE concentration reached 5%, the survival rate of HBE cells was <50%. The effect of CSE on HBE cell survival was revealed to be time and concentration-dependent (Fig. 1). CSE-induced DNA damage, was observed in the surviving HBE cells. In addition, benzopyrene-DNA adducts were detected in HBE cells after 24 h of 5% CSE treatment (Fig. 1).

HBE cells were treated with different concentrations of EGCG (0, 5, 10, 20 and 40 µM). The cell survival rate between each treatment group and the control was not significantly different (P>0.05). No apparent cytotoxicity was observed at any concentration of EGCG (Fig. 2). Compared with the CSE only treatment group, the HBE cells treated with 5% CSE+EGCG revealed a significantly higher survival rate. This indicated that EGCG protected HBE cells against CSE-mediated acute injury. The immunofluorescence assay revealed that HBE cells treated with CSE+EGCG formed less benzopyrene-DNA adducts than the CSE group. EGCG significantly reduced the formation of benzopyrene-DNA adducts induced by CSE exposure (Fig. 2).

HBE cell miRNA expression profiles were detected by microarray assay. The miRNA expression profiles of HBE cells treated with CSE were significantly different when compared with the expression profiles of untreated HBE cells. The expression of multiple miRNAs was upregulated (Table I), while the expression of several other miRNAs was downregulated (Table II). When HBE cells were treated with CSE and EGCG, the miRNA expression profile was significantly different compared with treatment with CSE only. EGCG treatment inhibited the CSE-mediated upregulation of several miRNAs (Table III). Moreover, new miRNAs were upregulated following EGCG treatment (Table IV).

These differentially expressed miRNAs were initially screened in HBE cells treated with EGCG and CSE. Non-small cell lung cancer, para-cancer, atypical hyperplasia and inflammatory tissues were collected and evaluated. miRNA levels were assessed by fluorescence in situ hybridization. This was performed to understand the clinical significance of the miRNA expression changes observed in the CSE-treated HBE cells. For example, miRNA-7114-5p was highly expressed in non-small cell lung cancer and atypical hyperplasia, with low expression in para-carcinoma and inflammatory tissues (Fig. 3). The difference was statistically significant (P<0.05).

Based on the original data, the functional miRNAs regulated by EGCG were screened using functional acquisition/loss analysis. A potential miRNA target gene had to be predicted by at least two predictive software (47-50). Targeted signaling pathways were predicted by the signal pathway analysis software 'Ingenuity Pathway Analysis' (http://www.ingenuity.com) (51,52). The bioinformatic analysis revealed that the CSE-mediated damage response of HBE cells involved multiple signaling pathways. The 'TGF-β signaling pathway', 'NOD-like receptor signaling pathway', 'cytochrome P450 pathway', 'p53 signaling pathway' and 'ErbB signaling pathway' were all targeted. The results of signaling pathway prediction were compared between the EGCG-treated group and the non-EGCG treated groups (Fig. S1). The protective effect of EGCG against CSE-induced damage was mediated by the NF-κB, TGF-β, p53, Bcl-2 and CYP signaling pathways. Conversely, in clinical pathological samples, TGF-β and CYP1A1 were revealed to be overexpressed in non-small cell lung carcinoma tissue and in atypical hyperplasia tissue, with low expression in para-lung carcinoma and chronic inflammatory lung tissue. NF-κB, on the other hand, had low expression levels in non-small cell lung carcinoma and atypical hyperplasia tissue, while being overexpressed in para-lung carcinoma and chronic inflammatory lung tissue (Fig. 4).

As in the previous experiment, the amount of water the rats drank varied slightly across the different experimental stages. However, the water consumed by the two groups of rats was roughly equal, with the water consumed by each rat averaging between 20 and 30 ml. Other conditions, such as food consumption, body weight and activity levels of the rats, were not significantly different between the EGCG-treated group and the EGCG-non-treated group. In the animal experiment, the rat lungs were stained with H&E before being assessed by two independent pathologists. After 4 weeks of passive smoke inhalation to the end of the experiment, chronic pulmonary inflammation and BE hyperplasia was evident. EGCG treatment significantly alleviated these CSE-induced lesions. There was no evidence of disease in the lungs of the control group (Fig. 5).

This experiment used immunofluorescence histochemistry to detect pulmonary benzopyrene-DNA adducts induced by CSE. After four weeks, there was fluorescence; this indicated the presence of benzopyrene-DNA adducts in the lung tissue of rats treated with CSE. The level of fluorescence increased gradually until the experimental endpoint. This demonstrated an increase in the number of benzo pyrene-DNA adducts in the lung tissue and BE cells of CSE-treated rats. Rats treated with CSE+EGCG revealed markedly weaker staining, suggesting they developed significantly fewer benzopyrene-DNA adducts compared with the CSE only treatment group. The control group developed no benzopyrene-DNA adducts across the full experiment (Fig. 6).

The mRNA expression levels of the target genes CYP1A1 and NF-κB were detected by RT-qPCR. CYP1A1 mRNA expression in the lung tissue of rats exposed to CS began to increase after four weeks of exposure. There was a gradual increase in the expression of mRNA across the full experiment, with the highest expression levels after 16 weeks of CS exposure. The mRNA level of CYP1A1was significantly lower in the EGCG-treated group across all time-points, when compared with the smoking only group (Fig. 7) (P<0.05). The NF-κB expression levels, following CS exposure, differed from that of CYP1A1. The level of NF-κB mRNA expression was increased after the fourth week. NF-κB expression was highest after 8 weeks of CS exposure. Following this, the expression level decreased. This pattern was also mirrored in the rats exposed to CS and treated with EGCG. At four and eight weeks, EGCG intervention led to significantly lower NF-κB expression compared with rats exposed to CS only (Fig. 7) (P<0.01).

Western blotting was used to detect the protein expression of CYP1A1 and NF-κB. Both CYPA1 and NF-κB proteins were at low levels in untreated rat lung tissue. After four weeks of treatment, CYP1A1 and NF-κB protein expression levels were increased in lung tissue treated with CS. Over the 16-week observation period, CYP1A1 protein expression levels increased in the lungs of rats treated with CS. Unlike CYP1A1, NF-κB protein expression in the lung tissues of rats treated with CS started to decrease after twelve weeks. Over the course of 16 weeks, EGCG downregulated the overexpression of CYP1A1 and NF-κB proteins in lung tissues of rats treated with CS (Fig. 8).

Lung cancer is a chronic disease that does not develop immediately upon exposure to a carcinogen (53,54), with chronic exposure to CS significantly increasing the risk of developing disease. It may take a long time between the initial carcinogen exposure to the onset of lung cancer (6). Tobacco contains carcinogenic substances such as benzopyrene. After smoking, benzopyrene binds to the DNA of epithelial cells and forms DNA adducts; this is considered to be a key step in the initiation of lung cancer (55,56). If the accumulation of benzopyrene-DNA adducts induced by cigarette smoking can be prevented, it may be possible to reduce the carcinogenic effect of benzopyrene. In the present study, there was significant formation of benzopyrene-DNA adducts in human BE cells treated with CSE. These results indicated the presence of active benzopyrene in CS. Smoking increases the risk of cancer developing in the epithelial cells of the trachea (57). However, the present study has revealed that epithelial cells exposed to CS in combination with EGCG, had a significant reduction in the amount of benzopyrene-DNA adducts formed. These results provided direct evidence that the green tea extract is protective against the formation of potentially cancerous adducts. In further in vivo experiments, it was observed that significant bronchial inflammation developed in rats after 4 weeks of CS inhalation, which was accompanied by the detection of benzopyrene-DNA adducts. This inflammation led to the development of BE atypical hyperplasia and heteroplasms in these rats. Importantly, these precancerous lesions were significantly reduced by the consumption of water containing 0.3% EGCG. Thus, it could be concluded that the green tea extract EGCG is protective against precancerous lesions and that EGCG interrupts a series of processes in the development of lung cancer, preventing carcinogenesis by mediating the damage caused by carcinogens found in CS.

As above-mentioned, lung cancer is a chronic disease, with the malignant transformation of BE cells being a slow process. There are numerous genes (such as NLRP3, Nrf2, IL-1β, caspase-1 and K-ras) involved in this transformation (58-60). It has been proposed that EGCG may interact in a protective manner with these numerous genes (61). However, the number of genes which play a key role in BE cell carcinogenesis may be few. Therefore, it was crucial to identify these genes and whether they may be modulated by the green tea extract EGCG. For the most part, aberrant gene expression was related to changes caused by the developing malignancy and not the carcinogenesis itself. Moreover, the expression of various genes and the activation of signaling pathways are regulated by miRNAs. Molecular changes, such as the dysregulation of miRNA expression, have been linked to tobacco smoking in lung cancer (35). In the present study, in human epithelial cells, it was observed that several miRNAs had upregulated expression following CSE treatment, with multiple miRNAs also being downregulated. Not only did the use of EGCG as a therapeutic inhibit the upregulation of potentially cancerous miRNAs following CS exposure, it also upregulated novel miRNAs that may play a protective role. Not all of the target genes of these miRNAs are related to carcinogenesis, however there are several genes which have been previously linked to the development of lung cancer (5,10,11,13,21,27). TGF-β, CYP1A1 and NF-κB are all targets genes of these miRNAs; their expression may also be affected by the intervention of EGCG. TGF-β and CYP1A1 were overexpressed in lung cancer tissues, while NF-κB was weakly expressed in atypical hyperplasia tissue and highly expressed in inflammatory tissues. It was indicated that the aberrant expression of TGF-β and CYP1A1 was closely related to smoking-induced lung cancer, while the aberrant expression of NF-κB may be more related to smoking-induced inflammation.

In the present study, rats exposed to CS had an initial bronchial/lung inflammatory response, followed by atypical proliferation and dysplasia of the bronchial epithelium. In the early inflammatory response to smoking, the expression of CYP1A1 and NF-κB was significantly upregulated; EGCG treatment significantly inhibited the overexpression of CYP1A1 and NF-κB. In the later experimental stages, the expression of NF-κB in the lung tissue from rats in the experimental group was not significantly different to that of the tissue identified in the control. This result further supported the hypothesis that NF-κB expression may be more correlated with the initial inflammation of the lung, rather than the development of tumors. In the CS treatment experiment, the expression of CYP1A1 in the lung tissue of the smoke-exposed rats was high, gradually increasing throughout the experiment. EGCG treatment consistently inhibited the overexpression of CYP1A1 induced by smoking in rat lung tissues. These results indicated that the mechanism of smoking-induced BE carcinogenesis was most probably related to the aberrant expression of CYP1A1; EGCG may therefore block smoking-induced BE carcinogenesis by regulating the function of CYP1A1. Compared with CYP1A1, the aberrant expression of NF-κB may be more closely associated with inflammation rather than with the carcinogenesis of BE cells.

CYP1A1 encodes the cytochrome P450 1A1. This protein is a major enzyme that activates polycyclic aromatic (pahs) carcinogens. Activated CYP1A1 can turn organic substances such as polyaromatic hydrocarbons into cytotoxins and other carcinogens, increasing the risk of cancer (62). Tobacco contains a large amount of benzopyrene, which is inhaled into the lungs when smoking. Benzopyrene is firstly epoxidized by CYP1A1, which is then hydrolyzed by epoxide hydrolase to form a dihydroxyl compound. This is then oxidized by CYP1A1 to form a diol epoxide. Diol epoxides have significant carcinogenic and mutagenic effects. These reactive metabolites produce DNA adducts, resulting in DNA mutations, gene expression profile alterations and tumorigenesis (62). Inhibition of CYP1A1-catalyzed benzopyrene metabolism may reduce the risk of smoking-induced lung cancer. In this in vivo experiment, it was observed that EGCG could inhibit the overexpression of CYP1A1 induced by smoking exposure. This therefore inhibits the metabolic mechanism of DNA adducts involving CYP1A1; subsequently preventing the development of atypical hyperplasia and heterogeneous precancerous lesions of bronchial epithelium. In addition to smoking, cooking, air pollution, automobile exhaust fumes and numerous other environmental sources may produce benzopyrene (62-65). There are still numerous opportunities for people to be exposed to environmental benzopyrene. Drinking green tea is therefore recommended as it is rich in EGCG which will inhibit the development of disease associated with benzopyrene exposure.