Hyperthermia induced HIF-1a expression of lung cancer through AKT and ERK signaling pathways
© The Author(s). 2016
Received: 21 June 2016
Accepted: 19 July 2016
Published: 26 July 2016
Hyperthermia is a promising treatment for human lung cancer, but recurrence of the primary lesion is common, as the residual tumor becomes adapted to heat treatment and growth is induced by hypoxia-triggered HIF-1a expression. Here, we explored the effects of hyperthermia on HIF-1a expression, proliferation, and lung cancer angiogenesis.
Human NSCLC NCI-H1650 and SCLC NCI-H446 cell lines were used to examine cell viability, apoptosis, and HIF-1a expression level under a gradient of thermal conditions (37, 42 and 47 °C for 40 min). The 47 °C heat-adapted NCI-H1650 and NCI-H446 sublines (also called NCI-H1650-b and NCI-H446-b cells) had enhanced viability and HIF-1a expression levels compared to the parental and 42 °C heat-adapted cells and were thus used for subsequent research. Concentration gradients of wortmannin and PD98095 were used to inhibit AKT and ERK expression, respectively in the NSCLC NCI-H1650-b and SCLC NCI-H446-b cell lines, and cell growth curves were drawn. Western blots were used to detect the expression of HIF-1a, extracellular signal-regulated kinase (ERK), protein kinase B (AKT), phospho-ERK, and phospho-AKT. We established a subcutaneous transplantation tumor model with wortmannin and PD98095 intervention. Immunohistochemistry was used to detect the expression of HIF-1a and the vascular specific marker CD34, and tumor growth curves were drawn.
Following hyperthermia treatment, HIF-1a expression in 47 °C heat-adapted NSCLC and SCLC cell lines was regulated by the AKT pathway. However, HIF-1a expression was also regulated by the ERK pathway in NSCLCs, while SCLCs did not exhibit changes in ERK. These biological behaviors are governed by signaling pathway protein phosphorylation. Furthermore, inhibiting the AKT pathway can suppress the proliferation and angiogenesis potential of both 47 °C heat-adapted NSCLCs and SCLCs, but inhibiting the ERK pathway only affects SCLCs.
Our study suggests that following hyperthermia, the proliferation and angiogenesis potential of residual NSCLCs and SCLCs is induced by HIF-1a. However, HIF-1a expression in NSCLCs is regulated by both the AKT and ERK signaling pathway, but HIF-1a expression in SCLCs is regulated only by the AKT signaling pathway. This study sheds light on the molecular regulatory mechanisms of lung cancer recurrence following hyperthermia treatment.
KeywordsAngiogenesis potential Cd34 Extracellular regulated protein kinases (erk) Hyperthermia Hypoxia-inducible factor-1 alpha (hif-1a) Non small cell lung cancer (nsclc) Protein kinase b (akt) Small cell lung cancer (sclc) Signaling pathway protein Tumor proliferation
In recent years, hyperthermia has been recognized as a clinical treatment for certain cancers (e.g. lung cancer), which can be induced by therapeutic techniques, such as radiofrequency ablation (RFA). However, one of the major problems with hyperthermia is that it is difficult to achieve complete tumor destruction using this technique, and recurrence is common, because the residual tumor is now adapted to heat treatment and growth is induced . Accumulating evidence indicates that both hypoxia and hypoxia-driven angiogenesis are the consequence of hyperthermia, and both of these factors play important roles in tumor growth . Under conditions of hypoxia, a signaling pathway involving a crucial oxygen response regulator, defined hypoxia-inducible factor (HIF), is turned on. HIF protein, especially HIF-1α and HIF-2α, are correlation with tumor development, metastasis and promote epithelial-mesenchymal transition . In contrast with HIF-2α, which is expressed in certain cell types of vertebrate species, the expression of HIF-1α is observed in most metazoan species and involved in the regulation of epithelial-mesenchymal transition of tumor . As a key transcriptional regulator, HIF-1α plays a central role in the adaptation of tumor cells to hypoxia and helps to regulate the expression of muitiple cytokines, such as vascular endothelial growth factor-A (VEGF-A), and promotes the proliferation  and angiogenesis potential  of small cell lung cancers (SCLCs). Earlier research also showed that HIF-1a is involved in apoptosis and the proliferation of non-small cell lung cancers (NSCLCs) [7, 8]. In our previous study, we found that local recurrences of SCLC following RFA treatment were driven by HIF-1a, while the thermal effects of RFA can promote the growth of residual NSCLCs by up-regulating HIF-1a expression .
The expression and activity of HIF-1a is not only induced in response to limited oxygen availability, but it is also modulated through related signaling pathways . Some studies have demonstrated that the expression of HIF-1a is regulated by major signaling pathways, including the extracellular signal-regulated kinase (ERK) pathway  and the protein kinase B (AKT) pathway . Intensive studies of the ERK and AKT pathways have revealed these signaling pathways play their most important roles in the molecular signaling network that governs growth, proliferation, differentiation and survival in many, if not all, cell types [13, 14]. Therefore, to uncover the molecular mechanisms of lung cancer recurrence following hyperthermia treatment, the present study explores the effects of hyperthermia on HIF-1a expression and cell proliferation and angiogenesis. We then went on to investigate the regulation and function of the Akt and ERK signaling pathways.
Chemicals and antibodies
Specific inhibitor wortmannin, PD98059, and Recombinant Human Heregulin were purchased from Sigma, St. Louis, MO, USA. TRIzol reagent was purchased from Invitrogen, Carlsbad, CA. RIPA lysis buffer was purchased from the Beyotime Institute of Biotechnology, China. The following primary antibodies: anti-CD34 (1:40 dilution), anti-HIF-1a (1:500 dilution), anti-ERK1/2 (1:1000 dilution), and anti-AKT (1:1000 dilution) were purchased from Wuhan Boster Biological Engineering Technology Limited Company. Anti-phospho-AKT (1:1000 dilution) was purchased from Cell Signaling Technology, Beverly, MA, USA. and anti-phospho-ERK1/2 (1:800 dilution) was purchased from Santa Cruz, CA, USA.
Cell culture, heat treatment of cells, and establishment of sublines
Human NSCLC NCI-H1650 cells and SCLC NCI-H446 cells were maintained in RPMI-1640 medium (Sigma-Aldrich Co., St. Louis, MO, USA) supplemented with 10 % fetal bovine serum (FBS), 100 units/mL penicillin, and 100 μg/ml kanamycin at 37 °C in a humidified atmosphere containing 5 % CO2 and 20 % O2. The medium was routinely changed 2-3 days after seeding. Cells were detached with trypsin/EDTA (GibcoBRL, Paisley, UK) and were resuspended in a 1:1 solution of serum-free RPMI-1640 medium to a final concentration of approximately 5× 105 cells/10 μl.
During the exponential phase, cells were exposed to hyperthermic stress in cell culture plates for 24, 48, or 72 h. The plates were sealed with parafilm and submerged in a water bath at the desired temperature for 10 min. The three desired temperatures were 37, 42, and 47 °C. The cells cultured at 42 and 47 °C generated 2 cell sublines each, named NCI-H1650-a and NCI-H1650-b; NCI-H446-a and NCI-H446-b respectively. After the hyperthermic treatment, fresh culture medium was added to each well, and the surviving cells were maintained at 37 °C with an atmosphere containing 5 % CO2 and 1 % O2 for 4 h. After determining cell viability and HIF-1a expression levels, we chose one subline for the following experiment.
TUNEL staining for apoptosis assay
Cells were grown on coverslips, treated with 5 μM BIX for 48 h and stained with Click-iT plus TUNEL assay kit (Invitrogen) according to previous study . Then, cells were washed with PBS, fixed in 4 % paraformaldehyde (PFA) for 20 min, and permeabilized with 0.25 % Triton X-100 for 15 min. The cells were incubated with TdT reaction buffer for 10 min, then TdT reaction mixture for 1 h, and then incubated with TUNEL reaction cocktail for 30 min. Incubation with 0.05 % Diaminobenzidine tetrahydrochloride (DAB) solution for 8 min was used for counterstaining. Cells were examined using a Nikon microscope with Image-Pro Plus 6.x software (Diagnostic Instruments, USA) for image analysis.
MTT assay for lung cancer cells viability
Cells were cultured at a concentration of 1 × 104 cells/well in 48-well plates. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) solution was added to each well at a final concentration of 0.5 mg/ml and incubated for 4 h. At the end of the incubation, formazan crystals, resulting from MTT reduction, were dissolved by addition of 150 ml DMSO per well. The optical density was read at 570 nm, and the average values were determined from replicate wells.
Growth of xenografts in nude mice
Male congenital athymic BALB/c nude mice were obtained from the Experimental Animal Center of the Shang Hai Jiao Tong University School of Medicine. They were maintained under pathogen-free conditions in accordance with established institutional guidance and approved protocols. All experiments were carried out using 6-8-week-old mice weighting 16-22 g. Sublines of NCI-H1650 and NCI-H446 cells were cultured in vitro (1 × 107), and a final concentration of approximately 5 × 105 cells/10 μl were suspended in PBS and subcutaneously injected into the flank area of mice. After tumors reached 3-5 mm in diameter, mice were injected with either vehicle (10 % DMSO/PBS), 4 mg/kg, or 5 mg/kg twice weekly. The tumor size was measured with calipers every 3 days, and tumor volume was calculated according to the formula: volume = width2 × length × 0.5. Tumors were removed and weighed 30 days after inoculation. All surgical procedures were performed under isoflurane inhalation anesthesia. Buprenorfine was injected intramuscularly prior to surgery for perioperative analgesia.
Immunohistochemistry detection for HIF-1a and vascular specific markers
All tumor tissue sections were cut into 4 μM sections, deparaffinized, and endogenous peroxidases were inhibited with 0.3 % hydrogen peroxide in methanol for 30 min. Antigen retrieval was achieved using 0.05 % protease XIV at 37 °C for 5 min. Sections were then incubated with a mouse anti-human HIF-1a or CD34 primary antibody overnight at 4oC. Next, the slides were incubated with biotin-conjugated rabbit anti-mouse secondary antibody at room temperature for 45 min. The sections were subsequently incubated with a streptavidin-biotin-peroxidase complex (Vectastain ABC kit, Vector Laboratories, Burlingame, CA, USA) at room temperature for 45 min. The reaction was visualized using chromogen diaminobenzidine (DAB) for 10 s. Finally, the slides were counterstained with hematoxylin and mounted. The slides were examined with a Nikon Eclipse Ti microscope under a 40X objective.
Western-blot analysis of HIF-1a and signaling protein
Cells and tissues were harvested and analyzed for the expression of HIF-1a, ERK, p-ERK, AKT, and p-AKT. Briefly, total protein was extracted by disrupting cells in RIPA lysis buffer and separating on a polyacrylamide gel and transferring to PVDF membrane. The membranes were then blocked at room temperature for 1 h with 5 % non-fat milk in Tris buffered saline containing Tween 20 (TBST). The membrane was incubated with anti-HIF-1a, anti-ERK1/2, anti-AKT, anti-phospho-AKT, and anti-phospho-ERK1/2 primary antibodies at 37oC for 2 h, and then with peroxidase-conjugated IgG at room temperature for 1 h. The membranes were subsequently incubated with goat anti-rabbit peroxidase-conjugated secondary antibodies, and immunoreactivity was detected by using an enhanced chemiluminescence kit, and captured on X-ray film. β-actin was used as an internal control.
The SPSS 13.0 software (SPSS, USA) was applied to complete data processing. An independent-samples t-test was used to evaluate the differences in optical density (OD) values or tumor cell numbers between groups with various treatments. All data are represented as the mean ± SD for three independent experiments. Results were considered statistically significant when the p-value was less than 0.05.
In vitro heat treatment can generate NCI-H1650 cell sublines with increased viability
Specific inhibitor wortmannin inhibited HIF-1a expression, and the proliferation, and angiogenesis potential of NSCLCs and SCLCs following 47 °C heat treatment
Specific inhibitor PD98095 inhibited HIF-1a expression, proliferation, and angiogenesis potential in NSCLCs but not SCLCs following 47 °C heat treatment
HIF-1a expression in the NSCLC cell subline adapted to 47 °C was induced by both AKT and ERK signaling
HIF-1a expression of the SCLC cell subline adapted to 47 °C is induced by the AKT, but not the ERK signaling pathway
Lung cancer is a heterogeneous, complex, and challenging disease to treat. Hyperthermia is an approach that takes advantage of the biological effects of heat to target tumors. Hyperthermia techniques have been the subject of extensive research with the overall goal of medicine development and equipment advancement . Now, hyperthermia is regarded as an effective treatment for lung cancer, which may be as successful as surgery, radiotherapy, and chemotherapy. At present, clinical hyperthermia treatment methods for lung cancers include laser ablation, radiofrequency ablation, and magnetic hyperthermia . Among these, radiofrequency ablation is becoming an increasingly accepted treatment for primary lung cancers in patients who are not candidates for subsegmental resection or lobectomy . The prognosis for tumor patients has been closely correlated with activation and expression level of HIF-1a which are regulated by many factors such as DEC2 (differentiated embryonic chondrocyte gene 2) . Besides this, heat treatment can cause hypoxia in the local tissue and increase HIF-1a expression levels, which can induce the over-proliferation of any residual tumors, leading to the recurrence of lung cancer . Additionally, the angiogenesis potential increased by heat-induced hypoxia can also play a role in the rapid growth of residual tumor cells that have escaped heat ablation. This phenomenon is often referred to as a “malignant transformation” . Hypoxia conditions present with, or induced by, heat treatment can be replicated in in vitro cell culture. The cell lines we used were already established and used in previous studies, so that further spontaneous transformation under normal culture conditions would be unlikely. Therefore, we concluded that the biological microenvironment associated with tumor growth changed due to the exposure to heat stress. Heat-adapted sublines became more proliferative, which became the focus of our subsequent work to identify the molecular/biological mechanisms involved in tumor recurrence.
In our previous study, HIF-1a was found overexpressed in many human cancers and various cell types, and the levels of HIF-1a activity were correlated with tumorigenicity, angiogenesis, and metastasis . Its target gene, VEGF-A, is mainly regulated by HIF-1a at the transcriptional level, and VEGF-A also plays a critical role in tumor angiogenesis, growth, and metastasis. Targeting the HIF-1a/VEGF-A axis may be a promising strategy for combating tumor recurrences following hyperthermia treatment . There has been a significant increase in the understanding of the importance of the signaling pathways that regulate the biological behavior of both NSCLCs and SCLCs (e.g. proliferation and angiogenesis) in recent years [25, 26]. Inhibitors of HIF-1a represent a new tool for improved cancer therapies . A number of chemical, protein, and nucleic acid inhibitors are included and classified based on their mechanisms of inhibitory action. Among these, inhibiting upsteam signaling to block HIF-1a expression has proven effective . HIF-1α is situated at the convergence of multiple oncogenic and tumor suppressor pathways, including the PI3K/AKT and MAPK/ERK pathways . These signaling pathways are at the heart of a molecular signaling network that governs growth, proliferation, differentiation, and survival in many cell types . They are dysregulated in various diseases, ranging from cancer to immunological, inflammatory, and degenerative syndromes, and thus represent an important drug target [31, 32]. A previous study found that activating the AKT and ERK signaling pathways could enhance HIF-1a/VEGF expression in some malignant tumors . From the study about the mechanical regulation of signaling pathway in lung cancer, some scholars find that inactivation of Akt signaling can inhibit the growth of human lung cancer cells through reducing SP1 and p65 protein expression . ERK and PI3K/AKT pathways can promote tumor cell growth and metastasis and a notable decrease of ERK and PI3K/AKT activation can be found in TRIM11 knocked down lung cancer cells . These results are in congruence with our results that show inhibiting AKT and ERK expression through specific inhibitors in NSCLs can down-regulate HIF-1a expression and inhibit angiogenesis. However, inhibition of ERK expression had no significant effect on HIF-1a expression in SCLCs, which was regulated by the AKT signaling pathways. We hypothesized that the prime cause for this observation was that the regulatory mechanisms governing tumor properties are different, based on histological origin. Therefore, we intend to investigate these regulatory mechanisms further in the future.
Hyperthermia is a promising treatment for human lung cancer, but local recurrence is common, as growth of residual tumors can be induced by thermal ablation. Our study demonstrates that hyperthermia inherently changes the properties of cancer cells, facilitating the creation of different cancer sublines. These sublines exhibited enhanced viability and angiogenesis potential, and we determined that HIF-1a/VEGF-A plays a central role during this biological process. Furthermore, we investigated the molecular pathways induced/affected by hyperthermia. We found that HIF-1a expression was induced in heat adapted cell lines and that in NSCLCs this involves both PI3K/AKT and ERK signaling pathways, while only the PI3K/AKT signaling pathway is affected in SCLCs. Altogether, we hope that through investigating the molecular mechanisms of lung cancer recurrence following hyperthermia, our work will supply additional evidence for the use of multidisciplinary synthetic therapies to treat lung cancer.
In this research we find that HIF-1a plays a critical role in the recurrence of lung cancer following hyperthermia treatment as the proliferation and angiogenesis potential of residual NSCLCs and SCLCs are induced by HIF-1a. However, HIF-1a expression in NSCLCs is regulated by both the AKT and ERK signaling pathway, but HIF-1a expression in SCLCs is regulated only by the AKT signaling pathway. Our study sheds light on the molecular regulatory mechanisms of lung cancer recurrence following hyperthermia treatment.
AKT, proteinkinase B; ERK, extracellular signal-regulated kinase; HIF-1a, hypoxia-inducible factor-1 alpha; NSCLC, non small cell lung cancer; SCLC, small cell lung cancer
We would like to thank the Research Center of the First Affiliated Hospital of Anhui Medical University and Laboratory Animal Center of Anhui Medical University for providing technical assistance. The authors would like to thank the Duoease Scientific Service Center for excellent language editing service and suggestions for figure revision.
JW and WW conceived and designed the study. JW and WW performed the experiments. WW analyzed the data. JW contributed reagents/materials/analysis tools. JW wrote the paper. WW read and revised the manuscript, accepted the final version. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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- Wang Y, Li G, Li W, He X, Xu L. Radiofrequency ablation of advanced lung tumors: imaging features, local control, and follow-up protocol. Int J Clin Exp Med. 2015;8(10):18137–43.PubMedPubMed CentralGoogle Scholar
- Wan J, Wu W, Chen Y, Kang N, Zhang R. Insufficient radiofrequency ablation promotes the growth of non-small cell lung cancer cells through PI3K/Akt/HIF-1alpha signals. Acta Biochim Biophys Sin (Shanghai). 2016;48(4):371–7.View ArticleGoogle Scholar
- Yang J, Zhang X, Zhang Y, Zhu D, Zhang L, Li Y, et al. HIF-2alpha promotes epithelial-mesenchymal transition through regulating Twist2 binding to the promoter of E-cadherin in pancreatic cancer. J Exp Clin Cancer Res. 2016;35:26.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang J, Zhu L, Fang J, Ge Z, Li X. LRG1 modulates epithelial-mesenchymal transition and angiogenesis in colorectal cancer via HIF-1alpha activation. J Exp Clin Cancer Res. 2016;35:29.View ArticlePubMedPubMed CentralGoogle Scholar
- Wan J, Ma J, Mei J, Shan G. The effects of HIF-1alpha on gene expression profiles of NCI-H446 human small cell lung cancer cells. J Exp Clin Cancer Res. 2009;28:150.View ArticlePubMedPubMed CentralGoogle Scholar
- Wan J, Chai H, Yu Z, Ge W, Kang N, Xia W, et al. HIF-1alpha effects on angiogenic potential in human small cell lung carcinoma. J Exp Clin Cancer Res. 2011;30:77.View ArticlePubMedPubMed CentralGoogle Scholar
- Fan LF, Diao LM, Chen DJ, Liu MQ, Zhu LQ, Li HG, et al. Expression of HIF-1 alpha and its relationship to apoptosis and proliferation in lung cancer. Ai Zheng. 2002;21(3):254–8.PubMedGoogle Scholar
- Swinson DE, O'Byrne KJ. Interactions between hypoxia and epidermal growth factor receptor in non-small-cell lung cancer. Clin Lung Cancer. 2006;7(4):250–6.View ArticlePubMedGoogle Scholar
- Wan J, Wu W, Zhang R. Local recurrence of small cell lung cancer following radiofrequency ablation is induced by HIF1alpha expression in the transition zone. Oncol Rep. 2016;35(3):1297–308.PubMedGoogle Scholar
- Zhang QL, Cui BR, Li HY, Li P, Hong L, Liu LP, et al. MAPK and PI3K pathways regulate hypoxia-induced atrial natriuretic peptide secretion by controlling HIF-1 alpha expression in beating rabbit atria. Biochem Biophys Res Commun. 2013;438(3):507–12.View ArticlePubMedGoogle Scholar
- Agani F, Jiang BH. Oxygen-independent regulation of HIF-1: novel involvement of PI3K/AKT/mTOR pathway in cancer. Curr Cancer Drug Targets. 2013;13(3):245–51.View ArticlePubMedGoogle Scholar
- Belaiba RS, Bonello S, Zahringer C, Schmidt S, Hess J, Kietzmann T, et al. Hypoxia up-regulates hypoxia-inducible factor-1alpha transcription by involving phosphatidylinositol 3-kinase and nuclear factor kappaB in pulmonary artery smooth muscle cells. Mol Biol Cell. 2007;18(12):4691–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Dent P. ERK plays the baddie (again). Cancer Biol Ther. 2013;14(11):997–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Klement GL, Goukassian D, Hlatky L, Carrozza J, Morgan JP, Yan X. Cancer Therapy Targeting the HER2-PI3K Pathway: Potential Impact on the Heart. Front Pharmacol. 2012;3:113.View ArticlePubMedPubMed CentralGoogle Scholar
- Ren A, Qiu Y, Cui H, Fu G. Inhibition of H3K9 methyltransferase G9a induces autophagy and apoptosis in oral squamous cell carcinoma. Biochem Biophys Res Commun. 2015;459(1):10–7.View ArticlePubMedGoogle Scholar
- Xu Q, Briggs J, Park S, Niu G, Kortylewski M, Zhang S, et al. Targeting Stat3 blocks both HIF-1 and VEGF expression induced by multiple oncogenic growth signaling pathways. Oncogene. 2005;24(36):5552–60.View ArticlePubMedGoogle Scholar
- Zhou J, Wang X, Du L, Zhao L, Lei F, Ouyang W, et al. Effect of hyperthermia on the apoptosis and proliferation of CaSki cells. Mol Med Rep. 2011;4(1):187–91.PubMedGoogle Scholar
- McTaggart RA, Dupuy DE. Thermal ablation of lung tumors. Tech Vasc Interv Radiol. 2007;10(2):102–13.View ArticlePubMedGoogle Scholar
- Hiraki T, Gobara H, Fujiwara H, Ishii H, Tomita K, Uka M, et al. Lung cancer ablation: complications. Semin Intervent Radiol. 2013;30(2):169–75.View ArticlePubMedPubMed CentralGoogle Scholar
- Hu T, He N, Yang Y, Yin C, Sang N, Yang Q. DEC2 expression is positively correlated with HIF-1 activation and the invasiveness of human osteosarcomas. J Exp Clin Cancer Res. 2015;34:22.View ArticlePubMedPubMed CentralGoogle Scholar
- Ke S, Ding XM, Kong J, Gao J, Wang SH, Cheng Y, et al. Low temperature of radiofrequency ablation at the target sites can facilitate rapid progression of residual hepatic VX2 carcinoma. J Transl Med. 2010;8:73.View ArticlePubMedPubMed CentralGoogle Scholar
- Obara K, Matsumoto N, Okamoto M, Kobayashi M, Ikeda H, Takahashi H, et al. Insufficient radiofrequency ablation therapy may induce further malignant transformation of hepatocellular carcinoma. Hepatol Int. 2008;2(1):116–23.View ArticlePubMedPubMed CentralGoogle Scholar
- Yao H, Wang H, Zhang Z, Jiang BH, Luo J, Shi X. Sulforaphane inhibited expression of hypoxia-inducible factor-1alpha in human tongue squamous cancer cells and prostate cancer cells. Int J Cancer. 2008;123(6):1255–61.View ArticlePubMedGoogle Scholar
- Wan J, Che Y, Kang N, Wu W. SOCS3 blocks HIF-1alpha expression to inhibit proliferation and angiogenesis of human small cell lung cancer by downregulating activation of Akt, but not STAT3. Mol Med Rep. 2015;12(1):83–92.PubMedPubMed CentralGoogle Scholar
- Jett JR, Carr LL. Targeted therapy for non-small cell lung cancer. Am J Respir Crit Care Med. 2013;188(8):907–12.View ArticlePubMedGoogle Scholar
- Inazu M, Yamada T, Kubota N, Yamanaka T. Functional expression of choline transporter-like protein 1 (CTL1) in small cell lung carcinoma cells: a target molecule for lung cancer therapy. Pharmacol Res. 2013;76:119–31.View ArticlePubMedGoogle Scholar
- Wan J, Wu W, Che Y, Kang N, Zhang R. Low dose photodynamic-therapy induce immune escape of tumor cells in a HIF-1alpha dependent manner through PI3K/Akt pathway. Int Immunopharmacol. 2015;28(1):44–51.View ArticlePubMedGoogle Scholar
- Gayed BA, O'Malley KJ, Pilch J, Wang Z. Digoxin inhibits blood vessel density and HIF-1a expression in castration-resistant C4-2 xenograft prostate tumors. Clin Transl Sci. 2012;5(1):39–42.View ArticlePubMedPubMed CentralGoogle Scholar
- Luo HY, Wei W, Shi YX, Chen XQ, Li YH, Wang F, et al. Cetuximab enhances the effect of oxaliplatin on hypoxic gastric cancer cell lines. Oncol Rep. 2010;23(6):1735–45.PubMedGoogle Scholar
- Liu B, Kuang A. Genetic alterations in MAPK and PI3K/Akt signaling pathways and the generation, progression, diagnosis and therapy of thyroid cancer. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2012;29(6):1221–5.PubMedGoogle Scholar
- Heavey S, O'Byrne KJ, Gately K. Strategies for co-targeting the PI3K/AKT/mTOR pathway in NSCLC. Cancer Treat Rev. 2014;40(3):445–56.View ArticlePubMedGoogle Scholar
- Ding M, Zhang E, He R, Wang X. Newly developed strategies for improving sensitivity to radiation by targeting signal pathways in cancer therapy. Cancer Sci. 2013;104(11):1401–10.View ArticlePubMedGoogle Scholar
- Liu LZ, Li C, Chen Q, Jing Y, Carpenter R, Jiang Y, et al. MiR-21 induced angiogenesis through AKT and ERK activation and HIF-1alpha expression. PLoS One. 2011;6(4):e19139.View ArticlePubMedPubMed CentralGoogle Scholar
- Chen Y, Tang Q, Wu J, Zheng F, Yang L, Hann SS. Inactivation of PI3-K/Akt and reduction of SP1 and p65 expression increase the effect of solamargine on suppressing EP4 expression in human lung cancer cells. J Exp Clin Cancer Res. 2015;34:154.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang X, Shi W, Shi H, Lu S, Wang K, Sun C, et al. TRIM11 overexpression promotes proliferation, migration and invasion of lung cancer cells. J Exp Clin Cancer Res. 2016;35(1):100.View ArticlePubMedPubMed CentralGoogle Scholar