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J Cancer 2022; 13(13):3434-3443. doi:10.7150/jca.77619 This issue Cite

Review

Clinical implications of the interaction between PD-1/PD-L1 and PI3K/AKT/mTOR pathway in progression and treatment of non-small cell lung cancer

Zihan Quan, Yang Yang, Hongmei Zheng, Yuting Zhan, Jiadi Luo, Yue Ning, Songqing Fan

Department of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.

✉ Corresponding author: Songqing Fan, Department of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China. E-mail address: songqingfanedu.cn.

Abstract

The discovery of immune checkpoints has been well known to provide novel clues for cancer treatments. Immunotherapy against the programmed cell death protein-1 (PD-1) /programmed death-ligand-1 (PD-L1), one of the most popular auxiliary treatments in recent years, has been applied in various tumor treatments, including non-small cell lung cancer (NSCLC). However, inevitable issues such as side effects and drug resistance emerge following the use of immune checkpoint inhibitors. The PI3K/AKT/mTOR pathway may participate in the regulation of PD-L1 expression. Abnormal PI3K/AKT/mTOR pathway activation results in increased PD-L1 protein translation, whereas PD-L1 overexpression can activate the PI3K/AKT/mTOR pathway inversely. Via downstream proteins, including 4E-BP1, STAT3, NF-κB, c-MYC, and AMPK in aberrant energy status, the PI3K/AKT/mTOR pathway can regulate PD-L1 post-transcription and translation. Besides, the regulation of the PI3K pathway by the PD-1/PD-L1 axis involves both tumor cells and the tumor immune microenvironment. Inhibitors targeting the PD-1/PD-L1 have been successfully applied in the treatment of gastrointestinal cancer and breast cancer. Meanwhile, drug resistance from alternative pathway activation also evidently affects clinical progress. To achieve a better therapeutic effect and quality of survival, the combination of multiple treatment modalities presents great research value. Here we reviewed the interaction between PD-1/PD-L1 and PI3K/AKT/mTOR pathway in the progression and treatment of NSCLC and summarized its clinical implications. The intracellular interactions between PD-1/PD-L1 and the PI3K/AKT/mTOR pathway indicate that PD-1/PD-L1 inhibitors have a wide range of potential applications. And we presented the mechanism for combining therapy with monoclonal antibody PD-1/PD-L1 and PI3K/AKT/mTOR inhibitors in this review, to broaden the therapies for NSCLC.

Keywords: PD-1/PD-L1, PI3K/AKT/mTOR pathway, Inhibitors, immunotherapy

Introduction

Lung cancer, primary non-small cell lung cancer (NSCLC), has ranked second in morbidity and first in mortality among cancer diseases worldwide, constructing a serious threat to human life and health [1]. With further study of the mechanism of tumorigenesis and the development of molecular detection, programmed cell death protein-1 (PD-1) /programmed death-ligand-1 (PD-L1) monoclonal antibodies have become the first-line therapy for advanced NSCLC patients [2]. Furthermore, the investigation of immunotherapy has become popular in cancer therapeutic research. Although some patients with PD-L1⁺ NSCLC have benefited from the application of PD-1/PD-L1 monoclonal antibodies markedly [3, 4], the side effects and drug resistance were still of great concern to patients [4]. Therefore, for patients with PD-L1⁺ in the advanced stage of NSCLC, combination therapy has become a considerable option, such as the combination of PD-1 monoclonal antibody pembrolizumab with platinum agents' chemotherapy [5]. The clinical trials of the third-generation EGFR-TKI osimertinib combined with PD-L1 monoclonal antibody durvalumab have achieved good experimental results [6]. The PI3K/AKT/mTOR pathway is an essential intracellular signaling pathway that regulates the processes of cancer diseases including cell metabolism, cell proliferation, apoptosis, and gene expression [7]. The PI3K/AKT/mTOR pathway is also reported to participate in the immunosurveillance of the tumor microenvironment [8]. Inhibitors of the PI3K/AKT/mTOR pathway have been under development and in clinical trials [9]. In this review, we will discuss the clinical implications of the correlation between PD-1/PD-L1 and PI3K/AKT/mTOR pathway activation in the progression and treatment of NSCLC, and explore the current situation of relevant targeted drugs and immunotherapy for NSCLC.

PD-L1 expression and PD-1 activation on tumor immunosuppression

NSCLC tumor cells usually express PD-L1 on the membrane and its receptor PD-1 is expressed on the membrane of CD8⁺ T cells [10]. The coexpression of PD-L1 and PD-1 inactivates CD8⁺ T cells [11], thereby suppressing anti-tumor immune activity [12]. Researchers find that the activation of PD-1 by PD-L1 inhibits transduction via inactivating the co-receptor CD28 [13]. In addition, CD4⁺Foxp3+ regulatory T cells (Tregs) belong to the immunosuppressive subpopulation of CD4⁺ T cells [14], while PD-1 expressed on their surface maintains the immunosuppressive function and enhances immune tolerance. CD4⁺ T cells are induced to differentiate towards Tregs by the activation of PD-1. And the high expression of Foxp3 mainly through inhibition of mTOR (mammalian target of rapamycin) increases the immunosuppressive effect as well [15]. It has been proved that several mechanisms encoded by CD274 can regulate the expression of PD-L1 [16], intracellular factors, and tumor microenvironment [17]. For example, PTEN influences PD-L1 expression by regulating the mRNA levels, while NF-κB induces PD-L1 gene transcription by directly binding to its promoter and other indirect ways [18]. Plenty of factors and pathways have been found to play a critical role in immunotherapy; more details are still under experiment exploration.

Anti-PD-1/PD-L1 immunotherapy for NSCLC patients with advanced stage

The anti-tumor immune function of T cells can be regained via anti-PD-1/PD-L1 drugs (Figure 1). For NSCLC patients with positive PD-L1 expression, immune checkpoint inhibitor therapy improves the patient's overall survival (OS) rate compared to traditional chemotherapy [19]. Immune checkpoint inhibitors now in clinical use or trials mainly contain the PD-1 monoclonal antibody, such as nivolumab and pembrolizumab [20], and the PD-L1 monoclonal antibody, including atezolizumab and durvalumab [21, 22]. Clinical trial studies have found that the median remission period and median OS significantly increase by using all those four drugs, and compared to conventional chemotherapy, the grade 3/4 adverse events (AEs) are significantly shortened to varying degrees [3, 4].

 Figure 1 

The schematic of PD-1/PD-L1 immunotherapy. T lymphocyte (T cell) plays an important role in killing cancer cells when surface T cell receptors (TCR) recognize and bind to the major histocompatibility complex (MHC) molecules. Programmed death ligand 1 (PD-L1, CD274) is a kind of immune checkpoint protein, which is highly expressed in part of tumor cells and promotes tumor cell escape from being killed by T-cell. Programmed death 1 (PD-1) expressed on T-lymphocytes can bind to PD-L1 and inhibits T cell proliferation and activity. When anti-PD-L1 drugs antagonized PD-L1 or anti-PD-1 drugs antagonized PD-1, the anti-tumor immune function of T cells recovered.

However, the application of a single PD-1 or PD-L1 monoclonal antibody remains flawed. First of all, the indications for only using one type of monoclonal antibody are limited [2, 23]. Nivolumab has been recommended in the NCCS guidelines as a follow-up treatment for metastatic non-squamous NSCLC after first-line chemotherapy or the tumor made progression after chemotherapy [2]. FDA has approved pembrolizumab as first-line therapy for patients with metastatic NSCLC and with PD-L1 expression levels ≥50% (with EGFR mutations, negative or unknown ALK rearrangement test results also available) [24]. Meanwhile, no contraindications (e.g., severe autoimmune disease or organ transplantation) are also required in these patients [25]. In one follow-up treatment for NSCLC [26], different from pembrolizumab, the use of atezolizumab required disease-related information about the patient, rather than the PD-L1 expression level detection. Phase III clinical trial of durvalumab has reported that those NSCLC patients who are unable to apply tumor resection surgically and with PD-L1 ≥25% using durvalumab after radiotherapy obtain significantly better prognosis than those receiving radiotherapy alone [27]. Secondly, tumor cells present resistance to immune checkpoint inhibitors [28] with natural and acquired resistance to PD-1 and PD-L1 inhibitors in various tumors such as melanoma, NSCLC, kidney cancer, and so on [29]. In addition, a certain degree of drug toxicity and side effects exist in any kind of PD-1 or PD-L1 monoclonal antibodies [30]. Therefore, as a popular research topic in recent years [31], the combination therapy of medicine shows great research value and clinical significance for broadening the scope of indications for immune checkpoint inhibitors, alleviating drug resistance, and mitigating the side effects of anti-cancer drugs including targeted drugs [32]. At this stage, the combination of immune checkpoint inhibition therapy with targeted drugs such as EGFR-TKIs [33] or platinum-agent chemotherapy is a popular way of combining therapies for intermediate to advanced NSCLC [34].

Roles of PI3K/AKT/mTOR pathway in tumor development

PI3K/AKT/mTOR pathway upstream gene PIK3CA amplification and PI3K, AKT mutations have been found in NSCLC tissues. The expression of all of these genes increased, while PTEN gene expression is absent, compared to paracancerous tissues [35]. Activation of the PI3K/AKT/mTOR pathway, which is related to multiple upstream and downstream elements, is associated with oncogenesis.

PI3K is an intracellular signal transduction protein with phosphatidylinositol 3- kinase activity, thus Class I PI3Ks are closely associated with cancer, and the PIK3CA gene is involved in encoding the subunits associated with this protein [36]. Overexpression of the PIK3CA gene can directly hyperactivate the PI3K/AKT/mTOR pathway [37]. The activation of PI3K is associated with overexpressed EGFR caused by EGFR gene mutations. The ERBB3 protein from the EGFR receptor tyrosine kinase family also drives PI3K activation. In some cases, EGFR family-related proteins in EGFR-mutant NSCLC can activate PI3K through roles of GAB adaptor proteins, independent of ERBB3 protein [38]. PI3K phosphorylates PIP2 and generates PIP3 then further activates AKT (protein kinase B) [39]. The activation of AKT phosphorylates corresponding enzymes and kinases and regulates a variety of downstream signaling pathways [40], which will indirectly promote the expression of the mammalian target of rapamycin protein (mTOR) [41]. On the contrary, PTEN promotes the conversion of PIP3 to PIP2 [42]. Moreover, the silence of the PTEN gene blocks the conversion of PIP3 to PIP2 [43] and enhances AKT activation [44]. MTOR is an element in two different multiprotein signaling complexes, mTORC1, and mTORC2, both involved in mediating apoptosis and proliferation in different ways [44]. Because of the complexity of the PI3K/AKT/mTOR pathway in regulating cell proliferation and apoptosis-related responses, inhibition of each of the responses in this pathway tends to activate the paracrine pathway, leading to the development of drug resistance [45].

Interaction between PI3K/AKT/mTOR pathway and PD-1/PD-L1

The PI3K/AKT/mTOR pathway can control PD-L1 expression. In lung squamous carcinoma or lung adenocarcinoma tissues with mutations in NRAS, KRAS, EGFR, BARF, PIK3CA, EML4-ALK, activation of PI3K/AKT/mTOR pathway and PD-L1 expression can be detected simultaneously [46]. PI3K/AKT/mTOR-related inhibitors (e.g. mTOR inhibitor rapamycin) decreased PD-L1 expression [47], while stimulation of enhanced AKT/mTOR expression increases PD-L1 expression (validated in mouse experiments) [48]. Multiple responses are linked between PD-L1 and PI3K/AKT/mTOR (Figure 2). For example, in lung squamous carcinoma, deletion of the PTEN gene is found to lead to higher PD-L1 protein translation, while PTEN gene expression deficiency simultaneously promoted AKT activation [49]. As downstream elements of AKT, β-catenin/TCF/LEF transcription complex stimulates CD274 gene transcription by binding to the PD-L1 promoter [50]. Meanwhile, the AKT downstream signaling protein NF-κB also acts on its promoter to induce PD-L1 mRNA expression [18].

 Figure 2 

PI3K/AKT/mTOR pathway regulating PD-L1 expression. PD-L1 expression is regulated by the PI3K/AKT/mTOR pathway, which controls numerous cell processes including PD-L1 translation and post-transcription. Arrows mean activation, and bars mean inhibition. While dotted lines represent PD-L1 expression and solid lines represent PI3K pathway functions. Phosphatidylinositol 3-kinases (PI3K) is activated by various factors including growth factor receptor tyrosine kinases. PI3K promotes phosphatidylinositol 4, 5-bisphosphate (PIP2) to generate phosphatidylinositol 3, 4, 5-trisphosphate (PIP3), and then activates Protein Kinase B (AKT). AKT mediated PD-L1 regulation is divided into two parts, activating β-catenin and activating the mechanistic target of rapamycin complex 1(mTORC1). β-catenin enhances PD-L1 expression by activating T-cell factor/lymphoid enhancing factor (TCF/LEF) and combining with the PD-L1 promoter. mTORC1 regulates PD-L1 promoter through signal transducer and activator of transcription 3(STAT3), mammalian target of rapamycin (NF-κB), and Myc, activated by beta-transducin repeat-containing protein (β-TrCP) and ribosomal protein S6 kinase beta-1(S6K1) mediated by MAX interactor 1(Mxi1) degradation. Also, mTOC1 induces ribosome biogenesis by promoting p70 protein S6 kinase beta-1(p70S6K1) and inhibiting eukaryotic translation initiation factor 4E-binding protein 1(4E-BP1). Both ways upregulate eukaryotic translation initiation factor 4E (elF4E), which promotes PD-L1 mRNA translation.

On the other hand, molecules like transcription factors including c-Myc [51] and transcription activating factor STAT3 may play a role in the post-transcription of PD-L1 [52]^. STAT3 phosphorylation is relevant to mTOR, but it remains unclear whether mTOR suppressed or promoted STAT3 activity. Some researchers reveal that the phosphorylation of STAT3 by mTOR leads to its maximal activation [53]. As for c-Myc, it has been reported that Mxi1/S6k/β-Trcp can activate c-Myc by promoting Mxi1 degradation and then work on downstream factors such as the CD274 gene [54]. One of the most important mechanisms of mTORC1 is regulating its downstream molecular S6 kinase. High expression of p70 S6 kinase also plays an important role in controlling the expression of PD-L1. The overexpression of mTORC1 can negatively regulate PD-L1 expression, while it suppresses β-TrCP-mediated proteasomal degradation of PD-L1 [55]. Besides, the activation of p70S6K can also promote the translation efficiency of PD-L1 mRNA in the ribosome via activating 4E-BP1. So at least four ways have been mentioned above to regulate PD-L1 expression. One of them is involved in regulating ribosome biogenesis and translation efficiency [56], while another one is referred to as the Mxi1/S6k/β-Trcp pathway [53]. It is supposed that the mTOR pathway may regulate PD-L1 expression through many of the ways mentioned above.

In turn, PD-1/PD-L1 can also regulate the PI3K/AKT/mTOR pathway (Figure 3). PD-L1 activates the PI3K/AKT pathway by stabilizing β-catenin [57], and overexpression of PD-L1 also increases the expression of p-AKT. For example, in gastric cancer, researchers confirm that the PD-1/PD-L1 axis can upregulate AKT phosphorylation [58]. According to another study, in glioma, cell-intrinsic PD-L1 binds to AKT preferentially when compared to other PI3K/AKT signal proteins. Suppressing cell-intrinsic PD-L1 then decreases phosphorylation of mTORC1 and p70S6K in melanoma [59] and ovarian cancer cells [60].

By the way, AMP-activated protein kinase (AMPK) has been reported to be involved in regulating the interaction between PI3K/AKT/mTOR pathway [61] and PD-1/PD-L1 because of aberrant energy status in cancer. Energy deprivation can affect anti-tumor immunity, induce AMPK to phosphorylate PD-L1, and decrease PD-L1 protein abundance [62]. On one hand, activated AMPK phosphorylates PD-L1 on its Ser283 site to block the combination of PD-L1 with CMTM4, a positive regulator of PD-L1, to induce its degradation [62]. On the other hand, researchers demonstrate that the activated AMPK phosphorylated S195 site of PD-L1 results in its abnormal glycosylation and degeneration [63]. Also, a previous study verifies that activated AKT can phosphorylate AMPK directly on its Ser485 site or indirectly on its Thr172 site [64], and down-regulate its expression. In conclusion, activating PI3K/AKT pathway can suppress the AMPK function and then induces a higher PD-L1 expression.

PD-1/PD-L1 activates the PI3K/AKT pathway not just in tumor cells but also in the immune microenvironment. It has been found in breast cancer that PD-1 on an element termed myeloid-driven suppressor cells (MDSC) immune microenvironment bound to PD-L1 on B cell can activate PI3K/AKT/NF-κB signaling pathway in B cell [65]. Then B cell stimulation hindered T cell immune response and promoted tumor cells' immune escape. On the contrary, in T cells, PD-1 collected downstream molecular SHP-2 which suppresses PI3K activation through targeting PTEN phosphorylation mediated by CK2 [66]. The phosphorylated PTEN is in a stable situation, resulting in lower PI3K/AKT expression. Although there is no direct evidence that high expression of PD-L1 is simply mTOR-dependent, it is well known that AKT/mTOR pathway activation can promote the immune escape of cancer cells by promoting high PD-L1 expression.

Value-added regulation of tumor cells by PI3K/AKT/mTOR pathway inhibitors

Several PI3K/AKT/mTOR pathway targeted therapeutic drugs mainly target related genes such as PIK3CA, AKT, TSC1/2, mTOR, PTEN, and so on [67]. Since the development of pathway targeted drugs lags behind the tumorigenesis mechanism research, currently many of them are still in clinical trials (Table 1). At this stage, drugs targeting PI3K are inhibitors of various PI3K isoforms. For example, alpelisib, a drug targeting PIK3CA mutant breast cancer in phase Ⅱ clinical trials [68] displays antitumor activity in pre-initiation studies. Copanlisib and duvelisib are FDA-approved for marketing for specific types of lymphoma or leukemia in the United States. ACP-319 (acertapharma), BYL719 (novartis), and serabelisib are also in clinical trials, but cytotoxic response occurs evidently with each of those drugs used alone [69]. Another discovery indicates that the antipsychotic agent flupentixol can inhibit lung cancer development via inducing apoptosis of oncocytes [70].

AKT inhibitors can be divided into two types: AKT competitive inhibitors and AKT aliasing inhibitors. The former competitively inhibits the ATP binding site on AKT and prevents AKT activation. While the latter inhibits AKT activation and phosphorylation by altering the chemical structure of the AKT PH structural domain, thereby preventing AKT localization on the cell membrane. AKT competitive inhibitors are majorly listed below: Capivasertib (AZD5363) [71], a selective PAN-AKT inhibitor that entered clinical trials for the treatment of breast, gastric, and prostate cancers; Afuresertib (GSK2110183) [72], a monotherapy of relapsed or refractory multiple myeloma treatment; Uprosertib (GSK2141795), which remains in phase Ⅰ and Ⅱ studies [73]; and the AKT inhibitor Ipatasertib (GDC-0068, RG7440), a monotherapy for the treatment of triple-negative breast cancer, still being in phase Ⅰ and Ⅱ studies [74]. Perifosine as an inhibitor of AKT metaplasia to inhibit neuroblastoma tumor cell growth has entered phase Ⅱ studies [75]. Meanwhile, the development of AKT inhibitors still encounters plenty of predicaments. The most notable one is that AKT plays a significant role in maintaining the dynamic balance of cellular physiological functions in normal tissues. AKT inhibitors can cause an unavoidable cytotoxic effort on normal tissues in cancer patients [76]. In addition, like other targeted drugs, the single use of AKT inhibitor tends to induce drug resistance and the substitution related to tumor formation.

There are three generations of mTOR inhibitors [77]. The first generation of mTOR inhibitors includes rapamycin, also known as sirolimus, approved by the FDA as an immunosuppressant and primarily used to prevent immune rejection in organ transplantation [78]. Ridaforolimus also belongs to the first-generation mTOR inhibitors [79]. Everolimus, and temsirolimus have little effect on mTORC2 [80]. Single-agent application of mTOR inhibitor such as everolimus has been applied to treat advanced neuroendocrine tumors, breast cancer, and non-functioning gastrointestinal, and temsirolimus is used to treat lymphangioleiomyomatosis [81]. The second-generation mTOR inhibitors such as Torin1 [82], work on ATP binding sites to block kinase activity of both TORC1 and TORC2 proteins, and PI-103, targets ATP binding sites of mTOR and PI3K. Whereas, drug development is still in the clinical research stage [83]. In contrast, newly developed third-generation mTOR inhibitors named rapalink-1 show potential usage in patients with first- and second-generation drugs resistant tumors [84].

 Figure 3 

PD-1/PD-L1 regulates PI3K pathway. The PD-1/PD-L1 regulates a number of functions of PI3K pathway. Both the transmembrane part and intracellular part of the PD-1/PD-L1 pathway participate in this process. Reactions can happen in both immune cells and tumor cells. Arrows mean activation, and bars mean inhibition. While dotted lines represent PD-L1 expression. In tumor cells, after PD-L1 mRNA translation, cell-intrinsic PD-L1 activates Protein Kinase B (AKT). After PD-1/PD-L1 binding, Src homology-2-containing protein tyrosine phosphatase 2(SHP2) promotes Phosphatase and tensin homolog (PTEN) phosphorylation through working on casein kinase 2(CK2), further promoting phosphatidylinositol 3, 4, 5-trisphosphate (PIP3) to generate phosphatidylinositol 4, 5-bisphosphate (PIP2).

Similar to other target agents, resistance can also happen when using PI3K/AKT/mTOR pathway targeted drugs [85]. After using mTOR inhibitors, for example, resistance occurs because of the activation of other tumor-related pathway elements and downstream of mTOR. An experiment shows that after being treated with everolimus or AZD8055, the mice obtained markedly increased activation in EGFR and MEK-ERK signaling pathway in tumor epithelial and stromal cells, respectively [86]. In the PI3K/AKT/mTOR pathway downstream, suppressing the expression or activation of mTOR may lead to the decrease of 4E-BP1 expression. 4E-BP1 suppresses eIF4E expression, and the overexpression of 4E-BP1 will make tumor cells sensitive to rapamycin as eIF4E plays a critical role in controlling translation [87] and tumor progression [88]. In summary, the new generation of target drug development and new combination therapies are under exploration [89].

Anti-tumor immune effects of PI3K/AKT/mTOR pathway inhibitors

The effect of the PI3K/AKT/mTOR pathway on immune cells and the immune microenvironment is complicated and combined with multiple pathways. PI3K/AKT/mTOR inhibitors affect the PD-L1 expression in cancer cells [8]. In NSCLC, the application of rapamycin results in a decrease in PD-L1 expression [47]. In the presence of interferon-γ (IFN-γ), inhibition of PI3K enhances the antitumor effect of IFN-γ, while IFN-γ expression positively is correlated with tumor infiltration of CD3⁺ T cells. However, IFN-γ also activates AKT/mTOR pathway in cancer diseases, and induces PD-L1 expression, antagonizing its antitumor effect [90]. In consideration of the cytotoxicity and resistance when single-use, PI3K/AKT/mTOR pathway inhibitors are of research interest in combination with other targeted drugs, such as the combination of inhibitors targeting two different components of the pathway. For example, the clinical trials of everolimus combined with EGFR-TKI for the treatment of advanced NSCLC show no significant improvement in therapeutic efficacy compared to EGFR-TKI alone. Nevertheless, the application of everolimus is still suggested for patients with EGFR-TKI-resistant NSCLC [91]. Therefore, further clinical trials of PI3K/AKT/mTOR pathway inhibitors in combination with targeted agents are needed.

PI3K/AKT/mTOR inhibitors also influence the antitumor effects of tumor immune cells infiltrating in cancers [92]. In the tumor environment, PI3Kγ protein expression inhibits NF-κB activity through AKT and mTOR while stimulating C/EBPβ activation in macrophages, resulting in suppression of antitumor immune effects [93]. Selective inhibition of macrophage PI3Kγ stimulates CD8⁺ T cell activation and enhances cytotoxic effects. Activating PI3K-mTOR signaling in T cells in the tumor environment suppresses autoimmunity by inhibiting activation and differentiation of common T cells and specializing in CD4+Foxp3+ regulatory T cells (Tregs) [94]. PI3K/AKT/mTOR inhibitors restore the anti-tumor immune effect of the body to some extent by blocking pathway activation.

PI3K/AKT/mTOR pathway and anti-tumor immunotherapy

As mentioned above, PI3K/AKT/mTOR pathway activation is closely related to PD-L1 expression and impacts the tumor immune microenvironment [95]^. The application of PD-L1 monoclonal antibodies enhances the antitumor immune effects of macrophages by inhibiting the AKT-mTOR pathway [96]. PD-L1 inhibitors have antagonistic effects on AKT and ERK1/2 activation to inhibit tumor proliferation [97]. So that blocking PD-L1 with antibodies in gastrointestinal mesenchymal tumors (GIST) can reduce CD8⁺ T cell depletion by regulating the PI3K/AKT/mTOR pathway to play an antitumor immune role [98]. Researchers find that in triple-negative breast cancer, atezolizumab can inhibit the mTOR signaling pathway by affecting P53-related genes [99]^. At the same time, both PD-1/PD-L1 monoclonal antibodies and PI3K/AKT/mTOR pathway inhibitors may develop resistance through activation of the bypass pathway, and have drug toxicity and side effects when achieving significant cancer suppression [100]. Overall, the combination drug application is a therapeutic modality that will be investigated further (Table 2). For instance, the combination of rapamycin and anti-PD-1 antibody has dampened the progression of NSCLC [47], with the pharmacological effect of rapamycin on inhibiting the activation of the AKT/mTOR pathway from differentiating CD3⁺ T cells [101]. While both drugs can alleviate the increased production of regulatory T cells (Tregs), PD-L1 enhances the role of Everolimus in the treatment of renal cell carcinoma [102].

Conclusion

This review discussed the tumor immunosuppressive effect of PD-1/PD-L1 inhibitors and the fundamental scenario of immune checkpoint inhibition therapy with the application of monoclonal antibodies. Taking NSCLC as an example, the review explained the components of the PI3K/AKT/mTOR signaling pathway and described their functions in driving carcinogenesis and suppressing antitumor immunity respectively. We also introduced the relevant immunosuppressive agents including the role and situation of single agent use in anti-tumor represented by everolimus, as well as the feasibility of combining multiple targeted agents and multiple adverse medication effects. The viability of a therapeutic strategy combining PI3K/AKT/mTOR pathway inhibitors with PD-1/PD-L1 inhibition will be considered. To date, research into PI3K/AKT/mTOR signaling pathway inhibitors is still currently in progress, and it exhibits great positive significance to investigate the interaction between PD-L1 expression and PI3K/AKT/mTOR signaling pathway activation for addressing anticancer drug resistance, prolonging tumor patient survival, and improving patient prognosis.

Acknowledgements

The work was supported by grants from The National Natural Science Foundation of China (No: 81773218, 81972838, 81703009, 82102805, and 82272722).

Competing Interests

The authors have declared that no competing interest exists.

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Author contact

Corresponding author: Songqing Fan, Department of Pathology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China. E-mail address: songqingfanedu.cn.

Received 2022-7-31
Accepted 2022-9-17
Published 2022-10-3

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