C33A(CL-0045), SiHa (CL-0210) and HeLa (CL-0101) cells were obtained from Procell. H8 cells were obtained from Qingqi (Shanghai) Biotechnology Development Co., Ltd. They were removed from liquid nitrogen and quickly put into a 37 °C water bath. After dissolving, the cells were transferred to a centrifuge tube containing 5 ml medium. The cells were collected by centrifugation, centrifuged at 1000 rpm for 5 min at room temperature, and the supernatant was discarded; The cells were suspended in the complete medium containing 10% fetal bovine serum, inoculated into the culture dish, gently blown and mixed, and cultured at 37 °C and 5% CO2 saturation humidity.

Quantitative real-time PCR is a method to measure the total amount of products after each polymerase chain reaction (PCR) cycle with fluorescent chemicals in a DNA amplification reaction. A method for quantitative analysis of specific DNA sequences in samples to be detected by internal or external reference. Total RNA was extracted from cells using TRIzol reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. For mRNA detection, first-strand cDNA was synthesized using a RevertAid first strand cDNA synthesis Kit (Thermo Fisher Scientific Inc., Waltham, MA, USA). All cDNA samples were individually configured for real-time quantitative PCR reaction systems. The system was configured as follows: SYBR Green 10 uL, upstream primer 1 ul, downstream primer 1 uL, dNTP 1 uL, Taq polymerase 2 uL, cDNA of the sample to be tested 5 uL, ddH2O 30 uL, total volume 50 uL, the solution was mixed by flicking the bottom of the tube, and briefly centrifuged at 6000 rpm. Place the prepared PCR reaction solution on the Realtime PCR instrument for PCR amplification reaction. The reaction conditions were as follows: predenaturation at 93 °C for 2 minutes, followed by 40 cycles of 93 °C for 1 minute, 55 °C for 1 minute, and 72 °C for 1 minute, with a final extension at 72 °C for 7 minutes. Relative gene expression was calculated automatically using 2-ΔΔCt. The primer sequences were showed in Table 1.

Collect protein sample preparation Use cell lysate to lyse adherent cells, suspended cells or tissue samples. Protein concentration was then determined for each protein sample. An appropriate amount of concentrated SDS-PAGE protein loading buffer was added to the collected protein samples. It is generally recommended to use low voltage constant voltage electrophoresis when the upper gel is used, while high voltage constant voltage electrophoresis is used when bromophenol blue enters the lower gel. Electrophoresis is expected to stop once the target protein has been properly resolved. Bio-Rad ‘s standard wet transfer apparatus was used with a transfer current set at 300-400 mA and transfer time of 30-60 minutes. Using Bio-Rad ‘s standard wet transfer apparatus, the transfer current can be set at 300-400 mA and the transfer time 30-60 minutes. Western blocking solution was added and blocked overnight at 4 °C. Phosphorylated protein was closed with 1% BSA. And then incubated overnight at 4 °C with mouse anti-human E-cadherin(1:5000, Sanying, Wuhan, CN), N-cadherin(1:5000, Sanying, Wuhan, CN), twist(1:1000, Abcam, Cambridge, MA, USA) and rabbit anti-human GAPDH(1:1000, Cell Signaling Technology, Danvers, MA, USA), snail(1:1000, Bioss, Woburn, MA, USA), p-p38(1:1000, Affinity Biosciences, OH, USA), p-JNK(1:1000, Cell Signaling Technology, Danvers, MA, USA), p-ERK(1:1000, Affinity Biosciences, OH, USA), p38(1:1000, Cell Signaling Technology, Danvers, MA, USA), JNK(1:1000, Cell Signaling Technology, Danvers, MA, USA), ERK(1:1000, Cell Signaling Technology, Danvers, MA, USA). After washing with TBST, the blots were incubated with horse radish peroxidase (HRP)-conjugated goat anti-rabbit or anti-mouse IgG(1:2000, Boshide, Wuhan, CN). Blots were visualized using ECL reagents (Pierce, Rockford, IL, USA) by a chemiluminescence imaging system (Bio-Rad, Richmond, CA, USA).

The human vector pLVX-mCMV-ZsGreen-IRES-Puro was obtained from Vinoser Biotechnology Co., Ltd. (Wuhan, CN). Human CLCA2 gene was amplified by PCR using plasmid CLCA2 as template. EcoRI and BamHI sites were introduced at both ends of primers. The connection between the large fragment of plasmid pLVX-mCMV-ZsGreen-IRES-Puro and human CLCA2 fragment, the ligation reaction was carried out at 22 °C for 3 hours. Take 10ul ligation product and 100ul JM109 competent bacteria, mix them in ice bath for 30 min, heat shock at 42 °C for 60s, put them on ice immediately for 2 min, add 400ul LB medium preheated to room temperature, culture them in constant temperature shaker at 37 °C for 1 h, centrifuge at 4000 rpm for 3 min, discard 400ul culture supernatant, mix the remaining 100ul with pipette, and evenly coat them on LB plate containing 100μg / ml ampicillin resistance, The cells were cultured upside down in 37 °C incubator overnight. Three single colonies were selected and inoculated in the medium containing 5 ml, 100 μg/ml ampicillin resistant LB medium. The plasmids were digested with EcoRI + BamHI, and the correct clones were selected for sequencing. The cell culture medium was changed and virus was added to infect the cells. After mixing, the cells were cultured continuously. After 8-12 hours, the cells were observed and replaced with fresh medium. After 3-4 days of infection, the fluorescence expression was observed, and the medium could be changed midway to maintain the cell activity. The infection conditions and parameters of target cells were confirmed by observing the effect of cell infection.

SiHa, HeLa and C33A were made into single cell suspension by DMEM, 2 × 105 cells were evenly seeded into the 6-well plate; Under the condition of 37 °C and 5% CO2 saturation humidity, the cells were cultured for 48 h; According to the titer of lentivirus, lentivirus was added to treat the cells for 72 hours. After lentivirus treatment, the cells were digested with 0.25% trypsin and blown into single cells. The cells were suspended in the medium for standby; The cell suspension was diluted and seeded in a 6-well plate with a density of 300 cells; Turn it gently to make the cells disperse evenly; The culture dish was placed in a 5% CO2 incubator at 37 °C for 2-3 weeks; When the clone appeared, the supernatant was discarded, washed with PBS twice and fixed with 70% ethanol for 15 min; Discard the fixed solution and add appropriate amount of crystal violet staining solution for 10-30 min; Clean with PBS and count.

Normal cells, NC (negative control) and -exCLCA2 lentivirus treated cells were added with 3 mL PBS to clean the cells, digested and collected with 0.25% trypsin, centrifuged at 1000 rpm for 5 min, supernatant was removed, and PBS was used to wash the residual serum twice; The cells were resuspended in serum-free DMEM medium and counted by cell counting plate. The cell concentration was diluted to 2.5 × 105 cells/mL in serum-free DMEM medium. 200uL cell suspension was added into the Transwell chamber, and cultured in 5% CO2 incubator at 37 °C; The Transwell was removed, the chamber was carefully cleaned with PBS, and the cells were fixed with 70% ice ethanol solution for 1 h; The cells were stained with 0.5% crystal violet dye, placed in room temperature for 20 minutes, PBS was cleaned, the non moving cells on the side of the upper chamber were wiped with clean cotton balls, and the microscope was observed and photographed.

The treated cells were washed with PBS twice, centrifuged at 1000 rpm for 5 min, and detected by flow cytometry according to the operation instructions of AnnexinV-APC/7-AAD cell apoptosis detection kit (Keji biology, Nanjing, CN). Joined 500 μL binding buffer, resuspend cells; Added 5 μL AnnexinV-APC, mix well and add 5 μL 7-AAD, mix well; Room temperature photoprotection reaction for 5-15 min (negative control was set at the same time, that is, normal cells were not added with annexin AnnexinV-APC and 7-AAD). Finally, flow cytometry was used for detection.

In the culture plate, the glass slide was soaked with PBS for 3 times, 3 minutes each time; The slide was fixed with 4% paraformaldehyde for 15 min, and the slide was soaked with PBS for 3 min each time; 0.5% Triton X-100 (prepared with PBS) was permeable for 20 minutes at room temperature (E-cad and n-cad were permeable for 5 minutes); The slides were soaked in PBS for 3 times, 3 minutes each time. The PBS was sucked dry with absorbent paper. Normal goat serum was dripped onto the slides and sealed at room temperature for 30 minutes; Each slide was dripped with enough diluted primary antibody and put into a wet box, and incubated at 4 °C overnight. Add fluorescent secondary antibody: PBST was used to soak the slides for 3 times, 3 minutes each time. After absorbing the excess liquid on the slides with absorbent paper, the diluted fluorescent secondary antibody was dripped and incubated in a wet box at 37 °C for 1 hour. PBST was used to soak the slices for 3 times, 3 minutes each time; DAPI was dripped and incubated in dark for 5 minutes. The specimens were stained with nucleus and PBST for 5 minutes. The redundant DAPI was washed off 4 times; Water absorbent paper was used to suck up the liquid on the climbing sheet, and the sealing liquid containing anti fluorescence quenching agent was used to seal the sheet, and then the images were observed and collected under the fluorescence microscope.

The SPF female nude mice were purchased from Changzhou cavens experimental animal Co., Ltd., weighing 18-21 g. The animals were divided into normal group, control group and overexpression group, each group had 3 nude mice, and the injected C33A cell volume was 5 × 10 [6]. Gently twist the skin under the right armpit with the left hand, hold a 1 ml syringe parallel to the skin with the right hand, insert the needle into the subcutaneous 1 mL, shake the needle from left to right, there is no resistance and see the needle move in the subcutaneous, indicating that the needle is in the subcutaneous. At this time, inject 100ul tumor cells into the subcutaneous, and gently press the needle eye position for a few seconds after withdrawing the needle to prevent the cells from flowing out. 28 days later, after anesthesia with intraperitoneal injection of 62.5 mg/kg pentobarbital sodium, the animals were sacrificed by dislocation and uniformly sent to Gansu Critically Ill Center for centralized treatment, and half of the tumor tissues were fixed and half frozen for follow-up study.

The paraffin embedded tissue sections were put into the staining VAT, and washed twice with xylene for 5 minutes each time. Three minutes each time with anhydrous ethanol, washed twice. Wash with 95 and 75% ethanol for 3 minutes each time. Wash with PBS for 5 minutes. Add proteinase K solution，at 37 °C reaction for 15 min to remove tissue protein. PBS 5 min each time, wash 3 times. PBS containing 3% H2O2 was added to the dyeing vat and placed at room temperature for 10 minutes. Wash with PBS 3 times, 5 minutes each time. After the excess liquid around the tissue section was carefully removed with filter paper, 2 drops of TdT enzyme buffer were quickly added to the section and placed at room temperature for 1-5 minutes. After carefully absorbing the excess liquid around the slice with filter paper, add 54 uL TdT enzyme reaction solution was put on the slices. Place the sections in the staining jar, add the washing and stopping reaction buffer that has been preheated to 37 °C, keep the temperature at 37 °C for 30 min, gently lift and put down the glass slide every 10 min, so that the liquid is slightly stirred. The sections were washed with PBS three times for 5 minutes each time. Two drops of streptavidin HRP working solution were added directly to the sections and placed in a wet box, reaction in dark for 30 min. Wash with PBS 3 times, 5 minutes each time. The newly prepared 0.05% DAB solution was added to the tissue sections and incubated at room temperature for 30s-5min. Wash with distilled water for 4 times, the first three times for 1 min each time, and the last time for 5 min. After 10 minutes of re staining with hematoxylin at room temperature, the slide was lifted up and put down in distilled water for 20 times, and then left standing for 30s. They were soaked with 70, 85, 95% absolute alcohol for 5 minutes. Xylene was dehydrated 2 min each time for 3 times. Then the film was sealed, dried and photographed under the microscope.

All experiments were performed at least in triplicate, and each experiment was independently performed at least 3 times. The graphical presentations were performed using GraphPad Prism 5.0. Data were presented as the means±SE and were analyzed using SPSS 21.0 software (Chicago, IL, USA). Statistical differences were tested by Chi-square test or two-tailed t-test. Differences were considered significant at P < 0.05 (*) or highly significant at P < 0.001 (**).