MicroRNA‑21 promotes the proliferation, migration and invasion of non‑small cell lung cancer A549 cells by regulating autophagy activity via AMPK/ULK1 signaling pathway

  • Authors:
    • Shuping Li
    • Xiaofei Zeng
    • Ruidong Ma
    • Li Wang
  • View Affiliations

  • Published online on: June 29, 2018     https://doi.org/10.3892/etm.2018.6370
  • Pages: 2038-2045
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Abstract

The present study investigated the expression of microRNA (miR)‑21 in non‑small cell lung cancer (NSCLC) tissues, its biological functions and mechanism of autophagy regulation. A total of 46 patients with NSCLC were enrolled in the present study. To measure the expression of miR‑21, reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR) was employed. NSCLC A549 cells were transfected with miR‑negative control (NC), miR‑21 mimics or inhibitor. The CCK‑8 assay was used to investigate the proliferation of A549 cells. To study migration and invasion abilities of A549 cells, The Transwell assay was performed. In addition, to determine the expression levels of ULK1, LC3B, AMPKα, p‑AMPKα and p62 proteins, western blotting was conducted and laser confocal microscopy was performed to observe the formation of autophagosomes in A549 cells. To explore whether miR‑21 regulates the biological functions of A549 cells via autophagy, an autophagy inhibitor, 3‑MA, or agonist, rapamycin, were used in a rescue assay. Results indicated that miR‑21 expression in NSCLC tissues was enhanced, and closely correlated with the occurrence and development of NSCLC. In vitro experiments showed that miR‑21 mimics promoted the proliferation, migration and invasion of A549 cells, while miR‑21 inhibitor inhibited these biological functions. Western blotting indicated that miR‑21 upregulated autophagy marker LC3BⅡ protein, but downregulated p62 protein. Laser confocal microscopy showed that miR‑21 activated autophagy of A549. Rescue experiments indicated that autophagy reversed the effect of miR‑21 on the proliferation, migration and invasion of A549 cells. Western blotting data suggested that autophagy‑related AMPK/ULK1 signaling pathway was activated by miR‑21, and interference or overexpression of ULK1 reversed the biological functions of miR‑21. The present study demonstrated that miR‑21 expression in NSCLC tissues was upregulated and positively correlated with lymphatic metastasis and clinical staging. In addition, miR‑21 regulated autophagy activity of NSCLC A549 cells via AMPK/ULK1 signaling pathway, and promoted the proliferation, migration and invasion of NSCLC A549 cells.

Introduction

Lung cancer is one of the most common malignant tumors in the world (1). It is usually derived from bronchial tip membranes or glands, and accompanied by regional lymph node metastasis or hematogenous dissemination (2). Approximately 1.8 million new cases of lung cancer are reported worldwide each year, accounting for 12.9% of all new cancer cases (3). Of note, the incidence of lung cancer in men is higher than that in women. One third of new and fatal cases of lung cancer occur in China, posing a great threat to human health (4). Most lung cancer cases are malignant epithelial tumors, including non-small cell lung cancer (NSCLC; 85%) and small cell lung cancer (15%) (5). The clinical symptoms of NSCLC are occult, and most patients have already got metastasis when they are diagnosed. Moreover, patients with successful surgery often develop tumor resistance, leading to chemoradiotherapy failure, tumor recurrence or even death (6). It is believed that effective inhibition of lung cancer proliferation, metastasis and drug resistance will greatly improve the prognosis of patients. However, the molecular mechanisms underlying the malignant phenotype of lung cancer cells still remain unclear.

MicroRNA (miRNA or miR) molecules is a class of non-encoding small RNA molecules (18–22 nucleotides) that inhibit the translation of target genes by binding with the 3′-untranslated region (UTR) of their mRNA (7). miRNA molecules play a role as oncogenes or tumor-suppressor genes in tumor proliferation, metastasis and drug resistance, being a type of important biomarkers and therapeutic targets (8,9). It is discovered that the expression of several miRNA molecules is abnormal in lung cancer, and closely related with the occurrence and development of NSCLC (6). For example, miR-30a-5p inhibits the resistance of NSCLC against paclitaxel by down-regulating the expression of Bcl-2 (10). In addition, miR-361-5p inhibits the proliferation and metastasis of NSCLC by targeting FOXM1 (11). miR-21 is a newly discovered miRNA molecule that is closely related with tumors (12). It is reported that miR-21 plays a role as an oncogene in NSCLC, and promotes the proliferation, invasion, metastasis and drug resistance of NSCLC (13,14). However, the mechanism of action of miR-21 is still unknown.

Autophagy is a catabolic process in which cells are subjected to stress such as hypoxia, starvation, and lack of nutrients (15). Autophagy acts as a ‘double-edged sword’ in tumorigenesis and development (16,17). On one hand, autophagy inhibits the occurrence and development of tumors by degrading abnormal components in cells or inducing non-apoptotic pathway death. On the other hand, tumor cells promote proliferation, invasion and metastasis through autophagy. Autophagy inhibitor chloroquine can greatly promote the death of tumor cells when used in combination with chemotherapy drugs (18). Studies show that miRNA molecules such as miR-181a and miR-140-5p are important in autophagy regulation (19,20). It is reported that miR-21 is able to regulate the drug resistance of NSCLC (21). Therefore, it is hypothesized that miR-21 may participate in the occurrence and development of NSCLC by regulating autophagy. In the present study, we investigate the molecular mechanism by which miR-21 regulates autophagy, and try to elucidate the role of miR-21 in the development of NSCLC.

Materials and methods

Patients

A total of 46 patients with NSCLC (age range, 24–76 years; mean age, 46.7 years) who received treatments at our hospital between October 2014 and 2016 were included in the present study. NSCLC and tumor-adjacent tissues were collected as experimental and control groups, respectively. The 46 NSCLC cases included 31 cases of adenocarcinoma, 13 cases of squamous cell carcinoma, and 2 cases of adenosquamous carcinoma. Patients with lymph node metastasis (29 cases) were included into N1 subgroup, while those without lymph node metastasis (18 cases) were included into N0 subgroup. In addition, 11 patients were at stage I, 17 patients were at stage II, 13 patients were at stage III, and 6 patients were at stage IV. None of the patients received radiochemotherapy or other antineoplastic therapies. None of the patients had history of other types of tumors. All procedures were approved by the Ethics Committee of Chengdu Medical College. Written informed consents were obtained from all patients or their families.

Cells

NSCLC A549 cells were cultured in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS) under 37°C and 5% CO2. When reaching 80–90% confluency, the cells were passaged. The medium was replaced every two days. Cells with passage numbers 3–6 were used for experiments.

A549 cells were divided into miR mimics-negative control (NC) group, miR-21 mimics group, miR inhibitor-NC group, and miR-21 inhibitor group. On the day before transfection, the cells (2×105) in log-phase growth were seeded onto 24-well plates containing antibiotics-free RPMI-1640 medium supplemented with 10% FBS. When reaching 70% confluency, 1.5 µl miR mimics-NC (random double-stranded RNA molecule; Hanbio Biotechnology Co., Ltd., Shanghai, China), miR-21 mimics, miR inhibitor-NC (random single-stranded RNA molecule; Hanbio Biotechnology Co., Ltd.) or miR-21 inhibitor (20 pmol/µl; Guangzhou RiboBio Co., Ltd., Guangzhou, China) and 1 µl Lipofectamine 2000 (Thermo Fisher Scientific Inc., Waltham, MA, USA) were added into two individual vials containing 50 µl Opti Memi medium, respectively. Five min later, the liquids in the two vials were mixed together before standing still for another 20 min. Then, the mixture was added onto the cells for an incubation of 6 h before changing to RPMI-1640 medium supplemented with 10% FBS. The cells were cultured at 37°C and 5% CO2 for 48 h before use.

Rescue experiments were performed in two ways. First, A549 cells (2×105) in miR-21 mimics and miR-21 inhibitor groups were seeded into 24-well plates containing antibiotics-free RPMI-1640 medium supplemented with 10% FBS. When reaching 70% confluency, the medium was replaced with the same medium containing 25 µM 3-MA and 100 nM rapamycin and cultured at 37°C and 5% CO2 for 24 h before rescue experiments. Second, A549 cells (2×105) in miR-21 mimics and miR-21 inhibitor groups were seeded into 24-well plates containing antibiotics-free RPMI-1640 medium supplemented with 10% FBS. When reaching 60% confluency, the cells were infected by 0.5 µg ULK1 eukaryotic expression plasmid (Hanbio Biotechnology Co., Ltd.) or its siRNA sequence. Cells in miR-NC group were infected by 0.5 µg NC plasmid. After being cultured at 37°C and under 5% CO2 for 6 h, the medium was refreshed to newly made RPMI-1640 medium containing 10% FBS before cultivation for 72 h. Then, the cells in each group were used for subsequent experiments.

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)

NSCLC and tumor-adjacent tissues (100 mg) were ground into powder using liquid nitrogen before addition of 1 ml Trizol isolation reagent (Thermo Fisher Scientific, Inc.) for lysis. After lysis, total RNA was extracted using phenol chloroform method. The purity of RNA was determined by A260/A280 using ultraviolet spectrophotometry (Nanodrop ND2000, Thermo Fisher Scientific Inc.). Then, cDNA was obtained by reverse transcription using miScript II RT kit (Qiagen GmbH, Hilden, Germany) from 1 µg RNA and stored at −20°C.

RT-qPCR was performed using miScript SYBR-Green PCR kit (Qiagen GmbH) and the reaction system was composed of 10 µl RT-qPCR-mix, 0.5 µl upstream primer (5′-ACAGCAGGCACAGACAGGCAGT-3′), 0.5 µl downstream primer (universal primer provided by the kit), 2 µl cDNA and 7 µl ddH2O. Reaction protocol was initial denaturation at 95°C for 10 min, and 40 cycles of 95°C for 1 min and 60°C for 30 sec.

Cell Counting Kit (CCK)-8 assay

The sample cells were inoculated in 96-well plates at a density of 2,000/well. At 0, 24, 48 and 72 h, 20 µl CCK-8 (5 g/l; Beyotime Institute of Biotechnology, Haimen, China) was added onto the cells. After being incubated at 37°C for 2 h, absorbance (490 nm) of each well was determined, and cell proliferation curves were plotted. Each group was tested in 3 replicate wells and the values were averaged.

Transwell assay

Matrigel chambers (Corning Incorporated, Corning, NY, USA) were used to determine the migration and invasion abilities of cells. Matrigel was first diluted with serum-free RPMI-1640 medium at a ratio of 1:2. In upper chamber, 50 µl diluted Matrigel was added and kept at 37°C for 1 h. Then, 1×105 cells and 200 µl serum-free RPMI-1640 medium were added into the upper chamber. In the lower chamber, 500 µl RPMI-1640 medium supplemented with 10% FBS was added. After incubation for 24 h, the cells in upper chamber were wiped by cotton swab. Then, the chamber was fixed using 4% formaldehyde for 10 min at room temperature, and then subjected to Giemsa's staining for 1 min. After washing for 3 times, cells that moved to the other side of the chamber were counted under a microscope (5 fields; magnification, ×200) to evaluate migration and invasion abilities.

Laser confocal microscopy

Cells in each group were seeded onto culture plates at a density of 2×105/well. When reaching 70% confluency, Ad-GFP-RFP-LC3B was added at a ratio of MOI=20. Seventy-two h later, the cells were observed under a laser confocal microscope (SP8; Leica Microsystems GmbH, Wetzlar, Germany). Green and red vesicles represented autophagy. The number of autophagy in cells was counted to evaluate autophagy activity.

Western blot analysis

Cells in each group were trypsinized and collected. Then, cold Radio-Immunoprecipitation Assay (RIPA) lysis buffer (600 µl; Beyotime Institute of Biotechnology) was mixed with the samples. Then, the mixture was lysed for 30 min on ice, and then centrifuged at 12,000 rpm and 4°C for 10 min. Bicinchoninic acid (BCA) protein concentration determination kit (RTP7102; Real-Times Biotechnology Co., Ltd., Beijing, China) was used to determine protein concentration in the supernatant. After mixing protein samples (6 µl) with 5× sodium dodecyl sulfate loading buffer, the mixture was denatured by boiling in water bath for 10 min. Afterwards, 10% sodium dodecyl sulfate-polyacrylamide gel electrophoresis (100 V) was performed using the samples. Then, the proteins were electro-transferred to polyvinylidene difluoride (PVDF) membranes on ice (250 mA, 1 h) before being blocked with 50 g/l skimmed milk at room temperature for 1 h. Afterwards, rabbit anti-human polyclonal ULK1 (1:1,000), LC3B (1:800), AMPKα (1:1,000), p-AMPK (1:800) and p62 (1:800) primary antibodies and mouse anti-human GAPDH (1:400) primary antibody (Abcam, Cambridge, UK) were added onto the membranes before incubation at 4°C overnight. Then, the membrane was extensively washed with phosphate-buffered saline with Tween 20 (PBST) for 5 times of 5 min, and incubated with goat anti-mouse horseradish peroxidase-conjugated secondary antibodies (1:4,000; Abcam) at room temperature for 1 h. Subsequently, the membrane was washed with PBST for 5 times of 5 min before the membrane was developed with enhanced chemiluminescence detection kit (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) for imaging. We used Image lab v3.0 software (Bio-Rad Laboratories, Inc., Hercules, CA, USA) to acquire and analyze imaging data. The relative expression of target proteins was expressed with the ratio against GAPDH.

Statistical analysis

All results were analyzed using SPSS v17.0 statistical software (IBM Corp., Armonk, NY, USA), and all data were shown as means ± SD. Paired Student's t-test was used to compare data between tumor-adjacent tissues and tumor tissues, while unpaired Student's t-test was performed to compare intergroup differences for lymph node metastasis and clinical staging. Multigroup measurement data were analyzed using one-way ANOVA. In case of homogeneity of variance, Least Significant Difference and Student-Newman-Keuls methods were used; in case of heterogeneity of variance, Tamhane's T2 or Dunnett's T3 method was used. P<0.05 was considered to indicate a statistically significant difference.

Results

miR-21 expression in NSCLC tissues is enhanced, and closely correlated with the occurrence and development of NSCLC

To determine miR-21 expression in NSCLC tissues, RT-qPCR was used. The data showed that miR-21 expression in NSCLC tissues was significantly higher than that in tumor-adjacent tissues (P<0.05; Fig. 1A). In addition, miR-21 expression in NSCLC tissues from patients with lymphatic metastasis was significantly higher than that in tissues from patients without lymphatic metastasis (P<0.05; Fig. 1B). Moreover, miR-21 expression in NSCLC tissues from patients at stages III/IV was significantly increased than that from patients at stages I/II (P<0.05; Fig. 1C). The result suggests that miR-21 expression in NSCLC tissues is enhanced, and closely correlated with the occurrence and development of NSCLC.

miR-21 expression promotes the proliferation of NSCLC A549 cells in vitro

To test the proliferation of A549 cells, CCK-8 assay was carried out. The data showed that absorbance of A549 cells that were transfected with miR-21 mimics was significantly enhanced than that in miR-NC group at all time points (P<0.05), while the absorbance of A549 cells in miR-21 inhibitor group was significantly decreased than that in miR-NC group at all time points (P<0.05; Fig. 2). The result indicates that miR-21 expression promotes the proliferation of NSCLC A549 cells.

miR-21 expression enhances the migration and invasion abilities of NSCLC A549 cells

To investigate migration and invasion abilities of A549 cells, Transwell assay was employed. The data showed that the expression of miR-21 in cells transfected with miR-21 mimics was significantly higher than that in cells transfected with miR mimics-NC (P<0.05), while expression of miR-21 in cells transfected with miR-21 inhibitor was significantly lower than that in cells transfected with miR inhibitor-NC (P<0.05; Fig. 3A). The number of cells in miR-21 mimics group that crossed chamber membrane in migration assay was significantly higher than that in miR mimics-NC group (P<0.05). By contrast, cell count in miR-21 inhibitor group that crossed chamber membrane in migration assay was lower than that in miR inhibitor-NC group (P<0.05). Similarly, cell count in miR-21 mimics group that crossed chamber membrane in invasion assay was higher than that in miR mimics-NC group (P<0.05). In addition, the number of cells in miR-21 inhibitor group that crossed chamber membrane in invasion assay was smaller than that in miR inhibitor-NC group (P<0.05; Fig. 3B and C). The results suggest that miR-21 expression enhances the migration and invasion abilities of NSCLC A549 cells.

miR-21 regulates autophagy activities of NSCLC A549 cells

To test the expression of autophagy-related proteins in A549 cells, western blotting was performed. Quantification of western blots showed that LC3B-II protein expression in miR-21 mimics group was significantly higher than that in miR mimics-NC group (P<0.05), while p62 protein expression in miR-21 mimics group was significantly lower than that in miR mimics-NC group (P<0.05). In addition, LC3B-II protein expression in miR-21 inhibitor group was significantly lower than that in miR inhibitor-NC group (P<0.05), while p62 protein expression in miR-21 inhibitor group was significantly higher than that in miR inhibitor-NC group (P<0.05; Fig. 4). The result suggests that miR-21 regulates autophagy activities of NSCLC A549 cells.

miR-21 expression facilitates the autophagy of NSCLC A549 cells

To observe the formation of autophagosomes in A549 cells, laser confocal microscopy was performed. The data showed that the number of autophagosomes in A549 cells of miR-21 mimics group was significantly higher than that in miR mimics-NC group (P<0.05), while that of miR-21 inhibitor group was significantly lower than that in miR mimics-NC group (P<0.05; Fig. 5). The result indicates that miR-21 expression facilitates the autophagy of NSCLC A549 cells.

miR-21 promotes the proliferation, migration and invasion of NSCLC A549 cells by regulating autophagy

To test whether miR-21 regulates the biological functions of A549 cells via autophagy, we used autophagy inhibitor 3-MA or agonist rapamycin. CCK-8 assay showed that treatment with 3-MA decreased the elevated proliferation of A549 cells that was induced by miR-21 mimics transfection to a level similar to miR-NC group (P<0.05; Fig. 6A). In addition, treatment with rapamycin increased the reduced proliferation of A549 cells that was induced by miR-21 inhibitor transfection to a level similar to miR-NC group (P<0.05; Fig. 6B). Transwell assay showed that treatment with 3-MA decreased the elevated migration and invasion abilities of A549 cells that were induced by miR-21 mimics transfection to a level similar to miR-NC group (P<0.05; Fig. 6C), while treatment with rapamycin increased the reduced migration and invasion abilities of A549 cells that were induced by miR-21 inhibitor transfection to a level similar to miR-NC group (P<0.05; Fig. 6D). The results suggest that miR-21 promotes the proliferation, migration and invasion of NSCLC A549 cells by regulating autophagy.

miR-21 regulates the autophagy of NSCLC A549 cells via AMPK/ULK1 signaling pathway

To further investigate the molecular mechanism by which miR-21 regulates autophagy, we predicted the target gene of miR-21 using TargetScan (http://www.targetscan.org/), but failed to discover any autophagy-related gene. Therefore, we examined autophagy-related signaling pathways using western blotting. The data showed that miR-21 up-regulated AMPKα subunit phosphorylation level and ULK1 expression (Fig. 7A). In addition, overexpression of miR-21 significantly increased the expression of LC3BII protein (P<0.05), but silencing of ULK1 by its siRNA significantly reduced the expression of LC3BII protein (P<0.05). By contrast, miR-21 inhibitor significantly decreased the expression of LC3BII protein (P<0.05), but overexpression of ULK1 significantly enhanced the expression of LC3BII protein (P<0.05; Fig. 7B). These results indicate that miR-21 regulates the autophagy of NSCLC A549 cells via AMPK/ULK1 signaling pathway.

Discussion

NSCLC patients often lose their best surgical chances because of extensive metastasis. Radiotherapy and chemotherapy can easily induce drug resistance of tumor cells and cause tumor recurrence and metastasis, leading to death of patients (22). Studies show that the development of NSCLC is a complex process involving multiple genes, multiple factors and multiple steps, such as gene mutation, abnormal expression, immunosuppression and tumor stem cells (23,24). Of note, miRNA molecules are involved in the regulation of various malignant phenotypes of NSCLC, and have become potential tumor therapy targets (25). In the present study, we discover that miR-21 expression in NSCLC tissues is significantly elevated, and positively correlated with lymphatic metastasis and clinical staging, suggesting that miR-21 may play a role as an oncogene. In vitro experiments demonstrate that miR-21 regulates autophagy of NSCLC cells via AMPK/ULK1 signaling pathway, and facilitates the proliferation, migration and invasion of NSCLC cells.

It is reported that miR-21 plays important roles in the occurrence and development of various malignant tumors. Expression of miR-21 is up-regulated in various human tumor tissues and cells, such as brain glioma, ovarian cancer, bladder cancer, prostate cancer, lung cancer, breast cancer, thyroid cancer, esophageal cancer, liver cancer, bile duct cancer, pancreatic cancer, colorectal cancer, gastric cancer, and B cell lymphoma. miR-21 participates in the proliferation, migration, invasion, differentiation and apoptosis of tumor cells (26,27). In addition, miR-21 is involved in the regulation of multiple downstream target genes such as PTEN, PDCD4, RECK, and TIMP-3 (21,28). Although there are many reports about the regulation of tumor cell proliferation, migration and invasion by miR-21, there is no literature report on whether miR-21 regulates autophagy activity in NSCLC. Our study shows that miR-21 is up-regulated in NSCLC, and is closely related to TNM staging and lymph node metastasis. In addition, miR-21 activates the autophagy of A549 cells by up-regulating LC3BII protein expression, down-regulating p62 protein expression, and increasing the number of autophagosomes in A549 cells. Of note, rescue experiments show that autophagy inhibitor or agonist can rescue the changes in biological functions of A549 cells caused by up-regulation or down-regulation of miR-21. This also suggests that miR-21 can exert its biological function of oncogene by activating autophagy.

Autophagy is closely related to the occurrence and development of tumors. It participates in the proliferation, metastasis and invasion of tumors mainly through three ways. First, autophagy provides energy for tumors and promotes tumor cell survival. Second, autophagy inhibits tumor cell apoptosis. Third, autophagy enhances the tolerance of tumor cells to radiotherapy and chemotherapy. For example, Pursiheimo et al (29) report that hypoxia induces autophagy and increases cell survival rate. Moon et al (30), show that autophagy protects ovarian cancer cells against metformin-induced apoptosis. Regulating autophagy activity has also become a new strategy for cancer therapy. AMPK signaling pathway is one of the key factors for intracellular and extracellular energy integration, and is closely related to autophagy. It is reported that AMPK increases cell survival rate by promoting autophagy via the up-regulation of ULK1 (31). In the present study, our data show that the phosphorylation level of AMPK α subunit is up-regulated, and the expression of ULK1, a key gene of autophagy, is increased, suggesting that miR-21 may regulate autophagy via ULK1. Consistently, siRNA interference and overexpression of ULK1 restore autophagy activity of A549 cells. The reason why we suspect LC3BII and ULK1 p-AMPK-alpha and LC3BII expression are different among the miR mimics-NC and miR inhibitor-NC groups is that miR mimics-NC is double-stranded and miR inhibitor-NC is single-stranded. The response of autophagy to the two sequences may be different.

The limitations of the present study include small sample size, and the subsequent lack of correlation analysis between miR-21 expression and N2/N3 lymph node status. In addition, the clinical correlation of miR-21 to NSCLC remains to be further verified. In future studies, we will use specific autophagy inhibitors to further verify the regulatory role of miR-21 on autophagy. In conclusion, the present study demonstrates that miR-21 is highly expressed in NSCLC tissues, and closely related to the occurrence and development of NSCLC. miR-21 can also activate autophagy via the AMPK/ULK1 pathway and play a role as oncogene. Therefore, miR-21 is a potential therapeutic target for NSCLC.

Acknowledgements

Not applicable.

Funding

This work was supported by the Project of Sichuan Provincial Health Bureau (grant no. 17PJ497).

Availability of data and materials

The analyzed data sets generated during the study are available from the corresponding author on reasonable request.

Authors' contributions

SL and LW collaborated to design the study. SL, XZ and RM were responsible for all experiments. SL and LW analyzed the data. All authors collaborated to interpret results and develop the manuscript. The final version of the manuscript has been read and approved by all authors.

Ethical approval and consent to participate

All procedures performed in the current study were approved by the Ethics Committee of Chengdu Medical College. Written informed consent was obtained from all patients or their families.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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September-2018
Volume 16 Issue 3

Print ISSN: 1792-0981
Online ISSN:1792-1015

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Spandidos Publications style
Li S, Zeng X, Ma R and Wang L: MicroRNA‑21 promotes the proliferation, migration and invasion of non‑small cell lung cancer A549 cells by regulating autophagy activity via AMPK/ULK1 signaling pathway. Exp Ther Med 16: 2038-2045, 2018
APA
Li, S., Zeng, X., Ma, R., & Wang, L. (2018). MicroRNA‑21 promotes the proliferation, migration and invasion of non‑small cell lung cancer A549 cells by regulating autophagy activity via AMPK/ULK1 signaling pathway. Experimental and Therapeutic Medicine, 16, 2038-2045. https://doi.org/10.3892/etm.2018.6370
MLA
Li, S., Zeng, X., Ma, R., Wang, L."MicroRNA‑21 promotes the proliferation, migration and invasion of non‑small cell lung cancer A549 cells by regulating autophagy activity via AMPK/ULK1 signaling pathway". Experimental and Therapeutic Medicine 16.3 (2018): 2038-2045.
Chicago
Li, S., Zeng, X., Ma, R., Wang, L."MicroRNA‑21 promotes the proliferation, migration and invasion of non‑small cell lung cancer A549 cells by regulating autophagy activity via AMPK/ULK1 signaling pathway". Experimental and Therapeutic Medicine 16, no. 3 (2018): 2038-2045. https://doi.org/10.3892/etm.2018.6370