TNF-alpha is a multicellular kinase that plays important role in various cellular events like cell differentiation, survival, and death. There are two types of this receptor; the first is TNFR1 that is expressed all over the cell and the second is TNFR2, which is expressed mainly in the immune cells. TNFR1 receptor contains the intracellular domain, the transmembrane domain, an extracellular domain, and it is considered as one of the important members of the death receptor family as it is mainly involved in the cell death program. Due to this, it is also considered a death domain (DD) receptor. TNFR2 does not contain the DD domain - its action mediates through TNFR1.^[5] The biological function of TNF executes through activating several signaling pathways like NF-κB and c-Jun N-terminal kinase (JNK). NF-κB produces a cell survival signal that produces an anti-apoptosis effect. There are various approaches like transgenic models, gene deletion, and use of antibodies that have been adopted to check the role of TNF-alpha in cancer. Data suggest that this receptor has an important role in the development of malignant cells. In the skin cancer study, it was found that TNFR1 mediated signaling activates NF-κB; which provides signals that help tumor cells to escape from apoptosis.^[6]

Interleukins functioned like intercellular hormones that can alter cellular functions. There are several types of interleukins (IL) that include IL-1, IL-6, IL-8, and IL-18 which play an important role in cancer development. IL-1α promotes cervical carcinoma and also induces anchorage independence in embryo fibroblasts. IL-1β also increases the cancer cell growth and is mainly associated with the development of chemoresistance in pancreatic carcinoma.‌^[7] Production of IL-6 is linked with p53; upon mutation of p53 produce a higher level of IL-6 and mainly involved in the cancers like multiple myeloma, non-Hodgkin’s lymphoma, bladder cancer, colorectal cancer, and renal cell carcinoma (RCC).‌^[8] Cytokine IL-8 has been reported to promote growth and metastasis of a wide variety of tumors. For tumor-associated inflammation, Ras-dependent IL-6 production is required. Expression of IL-8 by human melanoma cells and human ovarian cancer cells correlates with their metastatic potential. IL-8 has been detected in astrocytoma, anaplastic astrocytoma, glioblastomas, and central nervous system cervical carcinoma metastasis.^[9]

The chemokines family has four different members, which, based on the cysteine residues are classified as C, CC, CX3C, and CXC. Chemokines play either beneficial or non-beneficial role for cancer patients. Recruitment of mature dendritic and/or effectors cell provide beneficial effect while chemokine mediated recruitment of immature dendritic cell can increase tumor cell tolerance. In cancer cell development, chemokines play important role in the process like angiogenesis, inflammation, cell migration, etc.^[10] The main role of chemokines in inflammation is to traffic leucocytes to the inflammation site. CC chemokines play an important role in the macrophage and lymphocyte infiltration in melanoma and carcinoma associated with different cancers such as ovary, breast, cervix, and glioma. The concentration of chemokine receptor CXC4 and CCR7 was found higher in breast cancers. CXC play important role in inflammation, wound healing, cellular cycle regulation, angiogenesis, tumorigenesis, etc. The presence of CXCR4 was found in ovarian cancer while upregulation of CCR4 was found in renal cell carcinoma. CXCR4 activates EGFR in ovarian cancer.^[11]

Matrix metalloproteins are involved in various biological processes like inflammation, wound healing, cellular migration, skeletal formation, and cancer. MMP9 upregulation is found in various stages of tumorigenesis. MMP9 transferred by bone marrow plays a crucial role in skin carcinogens; supported by the evidence that transgenic mice lacking MMP9 have reduced hyperproliferation and invasiveness.^[12] In a breast cancer patient, 70 genes are identified for their poor prognosis; out of those two genes are MMP-1 and MMP-9. In a recent study, it was found that out of the 95 genes, MMP1 is the second most important gene which has the potential of breast cancer to produce lung metastases.^[13]

There are three isoforms of COX that have been identified: A) COX-1 is mainly involved in tissue homeostasis, platelet aggregation, renal blood flow, and maintenance of gastric mucosa, B) COX-2 is found in inflamed and neoplastic tissues, and C) COX-3 is mainly expressed in the brain and spinal cord. The COX pathway by PGH2 synthetase produces PGG2, which is unstable, and PGH2 in the presence of PGH2 synthase and peroxidase enzyme. This converts into various PGs and TxA2. COX-2 level in cancer can be elevated by cytokines, growth oncogene, and other factors. COX-2 is responsible for the development and growth of a variety of cancers.^[14] The expression of COX-2 is regulated by NF-κB. In colon carcinoma, the COX enzyme induces angiogenesis in two ways; the first way is modulation of angiogenic factors by COX-2 and COX-1 regulates angiogenesis in endothelial cells.^[15] COX-2 was found at a higher level in epithelial cells of invasive breast cancer. COX-2 also plays an important role in the growth of human lung adenocarcinoma. The physiological effect of PGs and TXA2 is mediated through G protein-coupled proteinoid receptors which are divided into nine different types. PGE2 gives biological response through four different receptors; EP1 to EP4. EP4 modulate PGE2, which is involved in the proliferation of colon cancer cells.^[16] Around 93% of melanomas are expressed with COX-2 with an expression ratio of around 68%. This overexpression plays important role in the development and growth of malignant epithelial cancer cells. In the pathogenesis of oesophageal cancer, involvement of both COX-1 and COX-2 have been detected due to their link with VEGF-A and VEGF-C, which are important modulators of angiogenesis.^[17]

The metabolic process for conversion of arachidonic acid to leukotrienes requires the presence of a 5-lipoxygenase enzyme which is the key factor for this metabolic process. Leukotrienes play important role in some allergic and inflammatory conditions. Apart from that, they are also involved in the pathophysiological functions of the brain like cerebral ischemia, brain edema, and increase the permeability of the blood-brain barrier in brain tumors.^[18] In the nude mice xenograft model treated with colon cancer with cigarette smoke extract, the inhibition of the enzymes COX-2 and 5-LOX reduces the tumor size.^[19] The evidence is further confirmed by the experiment in which cigarettes smoke without filter increases the expression of 5-LOX. This overexpression stimulates MMP and VEGF, which are key factors in the angiogenesis process. 5-LOX inhibitors decrease the colon adenoma formation and also decrease the expression of VEGF and MMP in tumor cells, ultimately the angiogenesis rate will be decreased.^[20]

Regulation of TNF, COX, LOX, and MMPs is done by the transcription factor NF-κB which is normally present in an inactivated state in most cells, but in cancer cells, NF-κB is found as active. The activation of NF-κB induces inflammation and tumorigenesis.^[21] The activation of the NF-κB response is triggered in the presence of pro-inflammatory cytokines and infectious agents. NF-κB heterodimer is trapped in the cytoplasm when it is bound to IkB, which, upon phosphorylation induces the cytokines, which results in activation of NF-κB. It has been found that in inflammation, the response of NF-κB is triggered through TNF-α which produces anti-apoptosis signals. By enhancing the signaling of NF-κB, cancer cells increase invasiveness. Cancer-associated TNF-α overexpression; inhibition of TNF-α suppresses the response of NF-κB and by this way produces apoptosis process.^[22] In the last few decades, extensive research has been going on NF-κB, and it was found that over-production of this receptor increases the resistance of chemotherapy as well as γ-radiation therapy. Inhibition of NF-κB can sensitize the cancer cells and therefore NF-κB is considered as one of the important targets for the development of chemotherapeutic agents.^[23]

Hypoxia-inducible factor contains two subunit alpha and beta; receptor present in the heterodimeric complex. The alpha subunit is less stable as compared to the beta subunit. Recent literature data have shown that inflammation (via inflammatory mediators) can also activate HIF-1 in normoxic conditions.^[24] Various cytokines, hormones can increase the expression of HIF-1. Cytokines such as IL-1β and TNF-α were reported for stimulation of HIF-1α expression. HIF-1α can stimulate the expression of several genes that includes, COX-2, iNOS, vascular endothelial growth factor receptor (VEGF), glucose transporter, etc.^[7] Overactivation of HIF-1α has been demonstrated in various types of cancer as it provides favorable conditions for the development and growth of tumor cells.^[25]

There are three different enzymes required for the synthesis of nitric oxide and iNOS is one of them. Cytokines like IL-1β, TNF-α, and IFN-γ can stimulate this enzyme. The expression of iNOS is regulated by transcription factors including NF-kB, activator protein 1, signal transducer and activator of transcription, 1α interferon regulatory protein 1, nuclear factor interleukin-6, and high motility group I (γ) protein.^[26] iNOS mediated cellular changes can produce malignancy, metastasis, angiogenesis of cancer cells which is involved in a variety of cancer types such as melanoma, prostate, bladder, and colorectal cancer.^[27]

STAT family includes seven members, which are involved in different cellular processes like survival, cell proliferation, and angiogenesis. Out of the seven members, the important member involved in cancer is the STAT3 transcription factor. The expression of STAT3 is stimulated mainly by IL6, IL-11, and other members of the cytokine family as well as growth factors. Upon activation, STAT3 phosphorylation followed by homodimerization occurs. This dimer shift into the nucleus binds with DNA and stimulates the transcription of some genes involved in oncogenic activation such as Bcl-2, CDK1, VEGF, etc. Due to this STAT3 is found highly expressed in several cancers like multiple myeloma, leukemia, prostate cancer, lymphoma, breast cancer, squamous cell carcinoma of the head and neck.^[28]

The other pathways which are directly or indirectly activated by inflammation or inflammatory receptors include mitogen-activated protein kinase (MAPK), phosphoinositide-3-kinase (PI3K), CREB signaling pathway, and Wnt/beta-catenin pathway. MAPKs are involved in various cellular processes like cell growth, differentiation, survival, and various immune and stress-related responses.^[29] It is mainly activated and regulated by various cytokines through the phosphorylation process. PI3K is mainly involved in the immune response of cancer cells and is found highly expressed in pancreatic cancer due to mutation of K-Ras in the patient with pancreatic cancer.^[30] CREB plays an important role in cell survival, differentiation of neurons, and metabolism. The process like reverse phosphorylation of serine by various kinase can increase the transcription activity of CREB. The high expression of CREB is found in various types of cancer which includes myeloid leukaemia, non-small cell lung carcinoma, melanoma, mammary carcinoma, etc.^[31] Wnt/beta-catenin pathway is involved in various biological processes like cell polarity, cell proliferation, and cell fate determination during embryonic development and tissue homeostasis. Wnt pathway can interact with many other pathways including HIF-1α, NF-kB, and Notch, stimulate the function of this pathway. Mutation of the Wnt pathway can produce various types of cancer which include cancers of the stomach, liver, intestine, pancreas, and ovaries.^[32]

The main role of NSAIDS as anticancer agents is due to their role of inhibition of COX1/2 enzyme which is required for the biosynthesis of prostaglandins and leukotrienes. The level of PGE2 is elevated in different types of cancer production. They increase cancer cell production by favoring angiogenesis, tumor growth, metastasis, and inhibiting apoptosis. PGE2 can activate several cellular pathways like MAPK, PI3K/AKT, and NF-kB which further activates VEGF, Bcl-2, EGFR, and MMPS and increase the rate of tumorigenesis. The possible mechanism for rational use of aspirin for cancer prevention involved inhibition of various targets like inhibition of COX1/2, certain pro-inflammatory cytokines, modulation on immune response, the effect on PI3K signaling, maintenance of cancer stem cell homeostasis, and decreased glycolytic rate in cancer cells.^[34] The long-term use of NSAIDs may lead to the development of several side effects such as renal failure, GI problems such as acidity, ulcer, and intestinal inflammation which cause perforation and strictures in small and large intestines. This factor can also induce the risk of cancer. To reduce the side effect of NSAIDs, they can combine with 5-LOX inhibitors so that the synthesis of prostaglandins and leukotrienes are blocked.^[35]

The investigation of the link between NSAIDs and cancer was done by Kune et al. The report suggests that patients taking NSAIDs had a significantly lower incidence of cancer. The positive results of NSAIDs in cancer prevention open a new direction in cancer research. The study was done on >1 million subjects with over 30 epidemiological studies; results suggest that NSAIDs can be prototypical agents in the prevention of cancer.^[34,36] Aspirin is a widely used drug in the world whose major role is in cardiovascular diseases. Multiple trials using aspirin for evaluation of anticancer properties have been done; data suggest that aspirin has approximately 20% to 25% ability to reduce incidence and mortality of several types of cancers. The major beneficial effects were found in the stomach, oesophageal and colorectal cancer. Other NSAIDs such as ibuprofen and piroxicam are able to reduce breast and colorectal cancer risk by showing a significant correlation between anti-inflammatory agent use and decreased cancer incidence. The other specific COX-II inhibitors drugs like rofecoxib and valdecoxib are under clinical investigation, but at the moment, these drugs are used as an adjuvant drugs because of their side effects.^[37–39]

Corticosteroids are used as anti-emetic agents to prevent nausea and vomiting driven by cancer chemotherapeutic agents. They are also effective as anti-inflammatory agents in various chronic inflammatory diseases. In the xenograft or experimental model of the breast, colorectal, glioma, and lung cancer. It was observed that pre-treatment with dexamethasone increases the effectiveness of chemotherapy. Dexamethasone was also found to decrease the incidence of lung tumors. The combination of dexamethasone with carfilzomib and lenalidomide had an advantageous effect in multiple myeloma patients.^[40,41]

Statins are used as anti-hyperlipidemic agents, which are also reported for their anti-inflammatory properties. The mechanism involved in the anti-inflammatory activity is due to the reduction of the pro-inflammatory cytokine, macrophage infiltration, and C-reactive protein. Due to additional anti-inflammatory properties, statins can reduce the risk of several cancers which include colorectal cancer, HCC, and breast cancer.^[42,43] Metformin, a drug used as an oral hypoglycaemic agent, is also reported as reducing the risk for several cancers, including colon, breast, lung, prostate, ovarian, and pancreatic cancers. Its antineoplastic effect is mediated through activation of the AMPK pathway, which counteracts the protumorigenic effect of hyperinsulinemia, the reduction of systemic glucose concentration, which counteracts the Warburg effect and through its anti-inflammatory properties.^[44] Embelin is an isoquinoline derivative reported for its anti-inflammatory properties due to its interference in the arachidonic acid metabolic pathway and can block 5-LOX and PGEs.^[45]