Regulation of Autophagy by Non-Steroidal Anti-Inflammatory Drugs in Cancer.

Cancer is the leading cause of death, placing a substantial global health burden. The development of the most effective treatment regimen is the unmet clinical need for cancer. Inflammation plays a role in tumorigenesis and progression, and anti-inflammation may be a promising option for cancer management and prevention. Emerging studies have shown that non-steroidal anti-inflammatory drugs (NSAIDs) display anticarcinogenic and chemopreventive properties through the regulation of autophagy in certain types of cancer. In this review, we summarize the pharmacological functions and side effects of NSAIDs as chemotherapeutic agents, and focus on its mode of action on autophagy regulation, which increases our knowledge of NSAIDs and cancer-related inflammation, and contributes to a putative addition of NSAIDs in the chemoprevention and treatment of cancer.

Introduction

Approximately 1.81 million new cancer diagnoses and 606,520 cancer-related deaths are projected to occur in the United States in 2020.1 Cancer research has focused on the identification of less toxic and more efficient therapeutic approaches to improve the overall prognosis of patients with cancer. Studies have shown that multiple modes of cell death and cell inhibition, other than apoptosis, contributing to chemotherapeutic efficacy.2 Autophagy is an evolutionarily conserved proteolytic process that involves lysosomal degradation and recycling of damaged cellular components and energy to maintain homeostasis.3,4 Autophagy is a survival mechanism of self-rescuing that favors the degradation of harmful and unwanted substances under stress conditions.5,6 Of note, autophagy is crucial for cell metabolism mechanism eliminating damaged organelles, proteins, lips and like that to maintain homeostasis and energy savings.7 By contrast, autophagic dysfunction contributes to various disorders including cancers, immune diseases, metabolic diseases, and neurological diseases.8–10 This review focuses on the recent progress of cancer in the regulation of autophagy.

Non-steroidal anti-inflammatory drugs (NSAIDs) exert antipyretic, analgesic, and anti-inflammatory effects.11 Although the chemical structures of these drugs differ, the therapeutic effects of NSAIDs are fundamentally similar due to decreased production of prostaglandins (PGs) through the inhibition of cyclooxygenases (COXs).12 Many experimental, epidemiological, and clinical studies have suggested that NSAIDs, particularly selective COX-2 inhibitors, may reduce cancer risk.13–15 It has been well established a mode of action that NSAIDs exert anticancer effects through induction of apoptosis, DNA damage repair, immune surveillance, and inhibition of tumor proliferation and invasion via COX-dependent or/and -independent pathways.16–20 NSAIDs regulate autophagy via Beclin1-dependent and Beclin1-independent pathways, which may result in anti-cancer effects.12,21 However, NSAIDs for cancer chemoprevention is on debate because the safety, efficacy, and doses of NSAIDs limit the clinical use in terms of cancer patients. Furthermore, the exact effects of NSAIDs on the regulation of autophagy are divergent according to the works of literature in different types and stages of cancer. Herein, we reviewed the pharmacological functions, side effects, and effects and mechanisms of NSAIDs including celecoxib, aspirin, sulindac sulfide, and meloxicam on autophagy regulation in cancer. This review may provide clues for the potential use and clinical trials of NSAIDs in the setting of clinical cancer treatment.

Pharmacological Activity of NSAIDs

Two forms of COX are present in tissues: constitutive COX-1 and inducible COX-2. The biological effects of COXs vary with tissue specificity, synthases, and the expression and regulation patterns. Both forms of COX are rate-limiting enzymes for the conversion of arachidonic acids and unsaturated fatty acids to PGs. COX enzymes convert arachidonic acid to PGH2, and generation of PGD2, PGE2, PGF2α, PGI2 or thromboxanes (TXA2).22,23 PGs produced by COX-1 regulate physiological processes such as hemostasis, stomach and kidney blood flow, and gastric acid secretion. COX-1 acts as a housekeeping gene and constitutively expressed in normal cells and tissues of platelet, blood vessel, mesothelial cells, stomach, and kidney. However, the COX-2 gene is not expressed in normal tissues (although expressed in the kidney). COX-2 expression is induced in inflammatory tissues by cytokines, lipopolysaccharides, and TNF-α. In tumors, COX-2 expression increased by up to 80%.24–26 PGs produced by COX-2 have important roles in inflammation, cell proliferation, angiogenesis, invasiveness, extracellular matrix adhesion, immune escape, and apoptosis inhibition in cancer.27,28 NSAIDs can be divided into two categories: non-selective COX inhibitors which inhibit COX-1/2, and selective COX-2 inhibitors. Non-selective COX inhibitors include aspirin, sulindac sulfide, acetaminophen, indomethacin, diclofenac acid, ibuprofen, naproxen, flurbiprofen, loxoprofen, hydroxybutanone, and piroxicam. Selective COX-2 inhibitors include celecoxib, meloxicam, rofecoxib, nimesulide, etc.29,30

Side Effects of NSAIDs

NSAIDs are also associated with a range of side effects that vary according to their COX inhibition selectivity.31–33 The side effects can be attributed to the systemic synthesis of PGs and local production of carboxylic acid. The major side effects in different systems are reviewed as follows. (1) In the gastrointestinal system, it was reported that serious gastrointestinal toxicity including upper gastrointestinal ulcers, gross bleeding, or perforation appeared to occur in patients for both long-term and short-term, with or without warning symptoms in the duration of NSAIDs administration. Minor upper gastrointestinal adverse effects such as dyspepsia, are common and occur at any time during NSAID therapy. Mechanically, the use of NSAID results in a reduction in the level of PGs that protects the membrane of the stomach from its acidic environment, making it susceptible to lesions. (2) Glomerular filtration rate and renal hemodynamics depend on COX-1, whereas salt and water excretion is mainly under the control of COX-2. NSAIDs treatment-related side effects of kidney damage through promotion of sodium and water retention, hypoxia, and ischemia via inhibition of PG production. Renal PGs have predominantly vasodilator effects on the kidneys. NSAIDs, especially indomethacin, have potential uses in various types of glomerulonephritis and nephrotic syndrome. The increased risk of analgesic nephropathy of chronic nephritis and renal papillary necrosis may be observed in the long term use of NSAIDs. (3) Hypertension, thrombosis, and increased risk of stroke, myocardial infarction, and heart failure are the main side effect of the cardiovascular system in the long term use of NSAIDs. COX-2 selective inhibitors have been shown to disrupt homeostasis between TXA2, which is produced by COX-1 and promotes platelet release and aggregation, and PGI2, which is produced by COX-2 and inhibits platelet release and aggregation from the endothelium. A large number of clinical trials and studies have aimed to determine safe doses of NSAIDs and evaluate their clinical potential.34 To minimize the potential risk for an adverse event, the lowest effective dose should be found in clinical practice and high-risk patients should be considered to receive alternate therapies that do not involve NSAIDs.

Decreased Cancer Risk and NSAIDs

Numerous experimental, epidemiological, and clinical studies have shown that NSAIDs decrease the risk of certain types of cancer.

Aspirin

Primary guidelines of NSAIDs for prevention of cardiovascular diseases in patients with colorectal cancer were established in the United States and worldwide, based on the high-level evidence of aspirin acting a beneficial role in cancer prevention.35 The results of six randomized trials and 26 case-controlled studies showed that aspirin was associated with reduced risk of colorectal cancer over a 20-year period.36 Recent epidemiological studies have shown that low-dose aspirin is more effective than high-dose aspirin at reducing morbidity and mortality associated with colorectal cancer.37 In 2011, a clinical trial by Rothwell et al (25,570 patients) showed significant correlations between long-term aspirin use and a lower risk of death resulting from gastrointestinal and solid tumors.38 Furthermore, other studies have demonstrated the beneficial effects of 5 or more years of regular aspirin use against colorectal, esophageal, pancreatic, stomach, cholangiocarcinoma, prostate, breast, pancreatic, and ovarian cancers.39–41

Non-Aspirin NSAIDs

Several non-aspirin NSAIDs, including celecoxib, sulindac sulfide, piroxicam, loxoprofen, and ibuprofen, have been shown to have anticancer effects. A randomized trial of patients with familial adenomatous polyposis (FAP) showed that sulindac sulfide and celecoxib inhibited the growth of adenomatous polyps and eliminated polyps in some cases.42 Celecoxib was approved by the US Food and Drug Administration in 1995 for prevention of colorectal adenomas and adenocarcinomas in patients with FAP.43 Besides, celecoxib can be used to prevent and treat breast, lung, prostate, stomach, head, and neck cancers.44 Similarly, loxoprofen was shown to inhibit the growth of implanted Lewis lung carcinoma in vivo.11 Furthermore, a study showed that ibuprofen treatment resulted in 40–82% inhibition of tumor growth and reduced liver metastases of colorectal cancer in vitro and in vivo. 45 Thereafter, the relationship between chronic inflammation and cancer has long been discovered in the retrospective studies of the use of NSAIDs in cancer treatment and prevention. The mechanisms of action by which NSAIDs exhibits its unique anticancer activity include inducing apoptosis and inhibiting proliferation and invasion of tumors by COX-dependent and COX-independent inhibition pathway are shown in Figure 1.

Figure 1

Nonsteroidal anti-inflammatory drug-induced anticancer effects via COX-dependent and COX-independent pathways.

Notes: Up arrow: promotion; down arrow: inhibition.

NSAID-Mediated Regulation of Autophagy

Many studies have shown that regulation of autophagy is an important mechanism associated with antitumor treatments.46,47 Therefore, we reviewed NSAID-mediated regulation of autophagy in cancer. Autophagy comprises the following four stages.48

Autophagy initiation. Extracellular or intracellular stress factors (hunger, insulin, growth factors, hypoxia, and endoplasmic reticulum stress) activate the PKA and PI3K/AKT signaling pathways; this results in inactivation of the AMPK signaling pathway and inhibition of mTOR, which can cause the release of ULK complexes (ULK1, ULK2, FIP200, ATG101, and ATG13) and activation of autophagy.

Vesicular nucleation. Phosphorylation of ULK complexes results in the activation of Vps34/Beclin-1 complexes. Class III PI3K forms a complex with Beclin-1 and other proteins (AMBRA1, ATG14, UVRAG) to form the phagophore. Binding of AMBRA1 to Beclin-1 stabilizes the class III PI3K complex, and binding of ATG14 and UVRAG to Beclin-1 enhances binding of Beclin-1 to VPS34, resulting in the formation of a double phagophore.

Vesicle elongation and completion. The phagophore complex drives nucleation and elongation to form annular vesicles; during this process, LC3-I is continuously converted to LC3-II under two types of ubiquitin-like conjugation system (Atg8/LC3-PE and Atg12-Atg5).

Autolysosome formation and degradation. In the presence of STX17, autophagosomes promote transport of degradable substances to lysosomes, resulting in the formation of autolysosomes. Autolysosomes play an important part in the degradation and circulation of damaging substances and energy. In vitro and in vivo studies have suggested that NSAIDs modulate autophagy in cancer via the classical Beclin-1-dependent pathway and a non-classical independent pathway. Specific mechanisms are shown in Figure 2.

Figure 2

Nonsteroidal anti-inflammatory drugs induce cytoprotection and suppress autophagy via Beclin-1-dependent and Beclin-1-independent pathways.

Notes: Black arrow: promotion; red arrow: suppression.

Classical Beclin-1-Dependent Signaling Pathway

BECN1, a homolog of yeast ATG6, is a candidate tumor suppressor gene and encodes the Beclin-1 protein, which is a well-established regulator of the autophagic pathway. Deletion mutations of the Beclin-1 gene occur in ovarian (75%), breast (50%), and prostate (40%) cancers.49 Beclin-1 is a component of the class III PI3K complex that promotes autophagy through regulation of autophagosome nucleation. Beclin-1 is regulated by the Bcl-2 anti-apoptotic family of proteins, and Beclin-1 binds to the BH3 domain of Bcl-2/Bcl-xL.50 Signaling of NSAIDs through the classical Beclin-1 dependent pathway interferes with the expression of Beclin-1 (in the case of nimesulide) and the Bcl-2 family of proteins (celecoxib and aspirin), dissociation of Beclin-1 from the Vps34/class III PI3K complex, conversion of LC3-I to LC3-II, and induction of autophagy.51,52

Non-Classical Beclin-1-Independent Signaling Pathway

The non-classical Beclin-1 independent pathway is composed primarily of the mTOR signaling pathway, which has a pivotal role in the induction of autophagy.53 NSAID targets upstream of the mTOR signaling pathway include PI3K/AKT, AMPK, and MAP kinases. The PI3K/AKT pathway negatively regulates mTOR signaling in the presence of various growth factors. NSAIDs (celecoxib, aspirin, ibuprofen, sulindac sulfide, and meloxicam) induce autophagy through the PI3K/AKT/mTOR signaling pathway, resulting in anticancer effects.54–56 AMPK is a key cellular metabolic sensor of AMP/ATP homeostasis and negatively regulates autophagy via the mTOR signaling pathway.57 Nutrient deficiency, low levels of endoplasmic reticulum stress, and reactive oxygen species (ROS) induce protective autophagy to promote cell survival and stability. Many studies have shown that NSAIDs (sodium salicylate and meloxicam) inhibit ER stress and ROS production, and disrupt the balance between cell death and cell survival via autophagy regulation in cancer. By contrast, some NSAIDs (celecoxib and OSU-03012) have been shown to induce ER stress and ROS production, resulting in autophagic tumor cell death.58 MAP kinases inhibit autophagy via the mTOR signaling pathway. Studies have shown that celecoxib activates JNK-mediated autophagic death, and aspirin promotes conversion from protective autophagy to autophagic death through p38.59,60 In addition, NSAIDs directly target the LC3-II, p62, p53, Atg5, Atg12, and HGF genes. p53, the most commonly mutated tumor suppressor gene in human cancers, positively regulates autophagy in DNA-damaged cells.61 Celecoxib directly upregulates p53-dependent DRAM to induce autophagy.62 Furthermore, NSAIDs have been shown to inhibit Bcl-2 and mTOR kinase through inhibition of the HGF/MET autocrine loop, which results in the induction of autophagy and decreased drug resistance.63 Nimesulide has been shown to directly upregulate LC3-II, Beclin-1, p62, Atg5-12, and p53, and induces autophagy to promote anticancer effects.64 Autophagy is a dynamic process in which autophagosomes are continuously formed and degraded, and studies have shown that NSAIDs (celecoxib and indomethacin) regulate autophagy by modulating autophagic flux in cancer.65,66

Regulation of Autophagy by NSAIDs in Cancer Therapy

Many studies have shown that induction of autophagy inhibits the development of tumors from premalignant lesions, and the initiation and inhibition of autophagy may be promising strategies to treat advanced cancers. In cancer cells, autophagy is a dynamic process that is regulated by the intracellular microenvironment in different tumor stage and tumor tape.67 Interestingly, NSAIDs induce anticancer effects and increase chemotherapy/radiotherapy sensitivity by inducing tumor-suppressive autophagy, and also regulate cytoprotective autophagy in combination with chemotherapeutic drugs to enable more efficacious treatment of apoptosis-resistant or drug-resistant tumors.

Celecoxib and Its Derivatives

Celecoxib selectively inhibits COX-2. In vivo and in vitro studies have shown that celecoxib has significant potential as an anticancer drug. Many studies have focused on the role of autophagy in celecoxib-induced apoptosis. These studies have evaluated whether celecoxib induces protective or deleterious effects based on cancer type, which has provided insights into its use as an anticancer agent.4,44,68

Celecoxib further enhances apoptosis induced by Bcl-2/Bcl-XL antagonists (ABT-737 and sabutoclax) via inducing autophagy in colon cancer and oral squamous cells.69,70 Celecoxib induces apoptosis and autophagy through the inhibition of the PI3K/Akt/mTOR signaling pathway, resulting in the inhibition of proliferation of tumor cells, including multidrug-resistant hepatoma cells.71,72 In addition, combination treatment with celecoxib and CPT-11 inhibited tumor growth in neuroblastoma through induction of autophagy.73 Moon reported that celecoxib induced autophagic death of p53 wild-type glioma cells through direct upregulation of p53, inhibition of DNA synthesis, and arrest of the cell cycle at the G1 phase.74 The ER stress response system has two distinct roles in NSAID-mediated autophagy. Under moderate stress, NSAID-induced autophagy is self-protective, such as in radio-resistant or drug-resistant tumor cells. Under strong cellular ER stress, NSAID-induced autophagy results in induction of apoptosis.75–78 Dimethyl celecoxib, a derivative of celecoxib, effectively inhibits colon cancer, triple-negative breast cancer, and glioma cell growth through induction of ER stress and in combination with chloroquine, bortezomib, and radiotherapy to play synergic effects on the induction of tumor cell autophagy.79,80 Celecoxib targets the pro-oxidative state of highly metastatic cancer cells and cancer stem cells and drives excess ROS production in these cells, resulting in cell death.81 OSU-03012 inhibits the proliferation of liver cancer through ROS-induced tumor-suppressive autophagy.59 Recently, studies have shown that celecoxib, 2,5-dimethyl-celecoxib, and OSU-03012 increase the sensitivity of multidrug-resistant cancer cells, including CD-44-overexpressing cancer cells, to Hsp90 inhibitors through activation of autophagy.82

By contrast, celecoxib in combination with chemotherapeutic drugs may be a more effective approach for cancer treatment through inhibition of autophagy. For example, inhibition of autophagy (3-MA or bafilomycin A1) increased celecoxib-induced apoptosis in human urothelial carcinoma cells. In addition, induction of autophagy (by rapamycin or GFP-LC3 transfection) alleviated celecoxib-induced cytotoxicity.83 Zhou et al reported that inhibition of autophagy enhanced celecoxib-induced apoptosis in osteosarcoma.85 Moreover, celecoxib inhibited autophagy through modulation of lysosomal function, which resulted in anticancer effects in HL-60 cells and increased the sensitivity of imatinib-resistant chronic granulocytes.66

Aspirin has been widely used as a clinical treatment. Regular use of aspirin can reduce the risk of cancer incidence, recurrence, metastasis, and mortality.17,85,86 Recent prospective studies showed that aspirin reduced the incidence of cancer through suppressive or cytoprotective autophagy and acted synergistically with chemotherapeutic agents. A number of studies have shown that aspirin downregulates Bcl-2, resulting in the autophagic death of human hepatoma, colon, and breast cancer cells. Huang et al reported that aspirin induced Beclin-1-dependent autophagy in human hepatocellular carcinoma cells.52 In addition, aspirin suppressed growth through induction of apoptosis and autophagy in PIK3CA-mutant colorectal cancer cells, a mouse liver cancer and sarcoma model, colorectal cancer, pancreatic cancer cells, and PI3K-mutant breast cancer.55,71,87 A recent study reported that 5-FU and anti-EGFR antibodies in combination with aspirin increased autophagy in a three-dimensional sphere culture system comprising HCT116 and HT29 colorectal cancer cells through increased autophagy.88 Autophagy has dual roles in cancer. Many studies have shown that autophagy can induce the development of tumors from premalignant lesions. By contrast, promotion or inhibition of autophagy may be an appropriate cancer treatment strategy during late-stage disease.89–91 For example, the long-term use of aspirin in combination with ABT-737 can induce lethal autophagy in lung cancer through the p38/MAPK signaling pathway. Furthermore, aspirin has been shown to induce protective autophagy in the early stages of non-small-cell lung cancer and autophagic death in the late stages of this disease.60 However, another study showed that aspirin inhibited autophagy and enhanced metformin-induced apoptosis of TPC-1 thyroid cancer cells.92

Sulindac Sulfide

Sulindac sulfide is clinically used for the treatment of rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. It is also used to treat gout and certain types of bursitis and tendonitis. A previous study showed that sulindac sulfide suppressed the growth of colorectal carcinoma HCA-7 and HCT-116 cells and xenografts.93 Regulation of autophagy by sulindac sulfide may be a promising novel cancer therapeutic strategy. Sulindac sulfide has been shown to inhibit the growth of lung adenocarcinoma cells through the induction of autophagy via the Akt/mTOR signaling pathway.94 Furthermore, sulindac sulfide increased the sensitivity of multidrug-resistant cancer cells to Hsp90 inhibitors through the induction of autophagy.75 Sodium salicylate inhibited the growth of A549 cells through the transformation from tumor necrosis to tumor-suppressive autophagy.95 Moreover, Bauvy et al reported that inhibition of autophagy increased sulindac sulfide-induced apoptosis in HT-29 cells.96,97

Meloxicam

Meloxicam has been shown to have anticancer effects against various malignancies.98 A previous study in hepatoma cells showed that meloxicam prevented apoptosis through induction of cytoprotective autophagy, and the autophagy inhibitor 3-MA promoted meloxicam-induced toxicity.99 Similarly, Zhong et al reported that meloxicam induced apoptosis and cytoprotective autophagy under conditions of low ER stress, and inhibition of autophagy increased the toxicity of meloxicam against hepatoma cells.100

Other NSAIDs

Other NSAIDs have been shown to regulate autophagy in cancer cells. For example, ibuprofen increased the sensitivity of multidrug-resistant cancer cells to Hsp90 inhibitors through the induction of autophagy.95 Nimesulide induced apoptosis and autophagy, resulting in aggravation of MPTP-induced neuroblastoma cell death.65 Piroxicam increased the cytotoxicity of carboplatin in human bladder cancer cells through the induction of autophagy.101 Consistent with these findings, indomethacin blocked autophagic flux through inhibition of lysosomal function, resulting in increased sensitivity of gastric cancer cells to indomethacin.67 These results demonstrate that the regulation of autophagy by NSAIDs plays an important part in anticancer therapy. Thus, the use of NSAIDs in combination with chemotherapeutic drugs may be a promising strategy for cancer treatment.

Conclusion and Future Perspectives

Anti-inflammation is believed to play a role in cancer management and chemoprevention. In the past few decades, research has shown that NSAIDs decrease the risk of certain types of cancer. The key mechanism of the protective action of NSAIDs is the inhibition of COX, which catalyzes the synthesis of PGs in inflammatory processes. In addition, NSAIDs exert anticancer properties and inhibition of tumor proliferation and invasion by inducing apoptosis, DNA damage repair, and immune surveillance in a COX-independent manner.20 However, epidemiological evidence of the association between NSAIDs uptake and the risk of cancer remains inconsistent and controversial. Based on the data that patients with non-aspirin NSAIDs uptake (HR = 0.81, 95% CI: 0.70–0.94), but not aspirin (HR = 0.77, 95% CI: 0.58–1.02), showed a statistically reduced the risk in hepatocellular carcinoma.102 Of note, the mechanism of NSAIDs in cancer prevention and treatment is still not clear, NSAIDs induce autophagy is a newly identified mechanism to explain the complicated effect of NSAIDs in cancer cells respond to stress induced by chemoradiotherapy. From the update results, a clear portrait emerges that divergent effect of autophagy induced by NSAIDs depends on tumor type, stage of tumorigenesis, tumor microenvironment, as well as genetic and epigenetic factors. Our laboratory data showed 2.5-dimethyl-celecoxib increases radiosensitivity in nasopharyngeal carcinoma by inhibiting autophagic flux (data not shown). Nowadays, persuasive evidence was reported to determine the fate of tumor cells treated with NSAIDs by molecular biology assays such as the interfering of autophagy inducer or inhibitor, autophagy-related gene over-expression and down-expression by plasmid, autophagy flux detection, and transgenic animal model in vivo. The relation between autophagy regulation and NSAIDs in cancer needs to more comprehensive laboratory investigation, and importantly a cluster of prospective, randomized controlled trials to determine the efficacy and safety of NSAIDs in common types of malignancy would be established to provide high-level evidence for clinical decision to support the combination treatment of NSAIDs and chemoradiotherapy or NSAIDs alone, which may be presenting a promising approach in the treatment of chemo- and radio-resistance tumors.