Open Access
Review
Issue
Vis Cancer Med
Volume 5, 2024
Article Number 3
Number of page(s) 6
DOI https://doi.org/10.1051/vcm/2024002
Published online 16 February 2024

© The Authors, published by EDP Sciences, 2024

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abbreviations

APCs: Antigen-presenting cells

CRT: Calreticulin

CD4+ TIL: CD4+ tumor infiltrating lymphocytes

DC: Dendritic cells

eNOS: Endothelial nitric oxide synthesis

ERK: Extracellular signal-related kinase

FasL: Factor related apoptosis ligand

Foxp3: Forkhead box p3

GRP170: Glucose regulated protein 170

GRP78: Glucose regulated protein 78

GRP94: Glucose-regulated protein 94

HLA-DR: Human leukocyte antigen DR

HSP: Heat shock protein

HSP90α: Heat shock protein 90α

HSPA5: Heat shock protein family A (HSP70) member 5

HSPB: Heat shock protein B

HSP-EX: HSP-bearing exosomes

HUVECs: Human umbilical vein endothelial cells

IDO: Intracellular indoleamine 2,3-dioxygenase

K5: Kringle 5

LOX-1: Lectin-like oxidized low-density lipoprotein receptor 1

LRP1: Low-density lipo-protein receptor related protein 1

LLC OVA: Ovalbumin-transfected lewis lung cancer

MIP-2: Macrophage inflammatory protein 2

MDSCs: Myeloid-derived suppressor cells

MHC: Major histocompatibility complex

MyD88: Myeloid-differentiation factor 88

NKG2C: Natural killer group 2 member C

NKG2D: Natural killer group 2 member D

NKp30: Natural killer receptor p30

SR-A: Class A scavenger receptor

TAM: Tumor associated macrophages

Th1: Type 1 CD4 helper T cells

TKD: Hsp 70 derived 14-mer peptide TKDNNLLGRFELSG

TLR-2: Toll-like receptor 2

TRAPs: Tumor cell released autophagosomes

VEGFR-2: Vascular endothelial growth factor receptor 2

Heat shock proteins (HSPs) are mainly induced by heat, radiation, infectious agents, heavy metal toxicity, and hypoxia. As molecular chaperones, HSPs are mainly categorized into several major families, including HSP40, HSP70, HSP90, HSP110, and HSPB (heat shock protein B), mainly distributed in the intracellular, endoplasmic reticulum and mitochondria [1]. In addition to their chaperone functions, HSPs also play important roles in cell signaling transduction, cell cycle, and apoptosis regulation in many diseases [2]. Recently, the stress-induced HSPs were reported to serve as endogenous danger signal molecules to enhance the immunogenicity of tumors and induce the response of CTL cells [3]. Many HSPs receptors on the surface of antigen-presenting cells were discovered, including CD91 or LRP1 (LDL receptor-related protein 1), CD40, LOX-1 (Lectin-like oxidized low-density lipoprotein receptor 1), CD36, TLR-2 (toll-like receptor 2), TLR-4 (toll-like receptor 4) and SR-A (class A scavenger receptor) [4]. HSPs play a crucial role in regulating the immune response of tumors. Many studies have shown that HSPs could carry tumor-related antigens and be released in the form of extracellular vesicles, regulating the function of immune cells in the tumor immune microenvironment and thereby affecting tumor cell growth [5]. It was reported that inhibiting the expression of HSP90 in tumors significantly reduces T cell surface receptors CD3, CD4, CD8, CD28, CD40L, and CD25, while CD2, CD11a, CD94, NKp30, NKp44, and NKp46 on the surface of NK cells were significantly activated [6]. The heat shock proteins HSP90, HSP70, and antigen-peptide complex can be processed by antigen-presenting cells (APCs) such as macrophages and dendritic cells (DC), then represented by MHC class I molecules [7]. Herein, we focus on the roles of HSPs in the tumor immune microenvironment and delineate the cross-talk between HSPs and immune cells as well as vasculature.

Heat shock proteins and T cells

HSPs bind to tumor antigen peptides to form a complex that is secreted and internalized by antigen-presenting cells such as macrophages and dendritic cells through endogenous pathways. They then bind to MHC-I molecules on the surface of antigen-presenting cells to activate CD8+. T cells. Studies have found that compared to simple tumor antigen peptides, HSP-bound antigen peptides have a stronger ability to activate CD8+. T cells through antigen-presenting [8, 9]. Endoplasmic reticulum chaperone glucose-regulated protein 170 (GRP170) is secreted by B16 melanoma as a danger signal molecule, inducing the secretion of IL-1β and TNFα by DC cells, simultaneously causing activation of antigen-specific CD8+. T cells [10]. Introducing GRP170 into B16 melanoma cells induces anti-tumor immunity and suppresses distant lung metastasis of B16 melanoma [10]. Infiltrating CD8+. T cells were increased and IFN-γ and IL-12 accumulated around tumor cells [10]. Also, HSP70 purified from human melanoma cells activates CD8+. T cells in an antigen- and HLA class I-dependent fashion [9]. GP96 (glucose-regulated protein 96) secreted from ovalbumin-transfected Lewis Lung Cancer (LLC OVA) cells activated DC cells, leading to a significant increase in cytotoxic CD8+. T cell activity in mouse spleen cells. OVA-specific (+) CD8+. T cells were mainly recruited near lymph nodes after activation [11].

CD4+ T cells are divided into Th0 cells secreting IL-2, IL-4, and IFN-gamma, Th1 cells secreting IL-2 and IFN-gamma, and Th2 cells secreting IL-4 [12]. In the tumor microenvironment, the tumor antigen-HSP70 complex is recognized by the HLA class II molecules on the APCs (antigen-presenting cells) surface. After antigen presentation, the tumor-specific CD4+ TIL (CD4+ tumor infiltrating lymphocytes) recognizes the HLA class I – or II on the surface of antigen presenting cells, resulting in a direct cytotoxic effect on tumor cells [12, 13]. Heat shock protein 90α (HSP90α) expressed on the surface of tumor cell-released autophagosomes (TRAPs), then secreted from tumor cells to stimulate CD4+ T cell by production of IL-6 via TLR2-MyD88-NF-κB signal cascade, thereby promoting tumor growth and metastasis [14]. BALB/c mice were immunized with exosomes containing HSP70 and type 1 CD4+ helper T (Th1) cell responses were stimulated and a large amount of IL-2 and IFN-γ were produced [15]. The immunogenic HSPs including GP96, HSP70, and calreticulin (CRT) can bind to CD91 on APCs for cross-presentation of the HSP-chaperoned peptides and lead to priming of T helper cells [16]. HSPA5 (heat shock protein family A (HSP70) member 5), also known as glucose-regulated protein 78 (GRP78), is an evolutionarily highly conserved protein. It is also an immunomodulator able to arrest inflammation through induction of tolerogenic DCs and subsequent generation of T regulatory cells. More HSPA5-treated DCs expressed amounts of intracellular indoleamine 2,3-dioxygenase (IDO) and produced copious amounts of IL-10. T cells co-cultured with HSPA5-treated DCs developed regulatory function with increased surface expression of CD4(+) CD25(hi) CD27(hi) but with no concomitant increase in Foxp3 (forkhead box P3) [17]. Taken together, HSPs can bind to tumor antigen peptide and stimulate antigen-presenting cells and finally induce T cell infiltration in the tumor microenvironment.

Heat shock proteins and B cells

In addition to regulation of T cells, HSPA5 plays an important role in regulating B cells and other inflammatory processes. HSPA5 can induce IL-10-producing splenic B cells and B cells highly expressing PD-L1 and FasL. B cells treated with HSPA5 and anti-CD40 can lead to suppression of T cell proliferation [18]. GRP94 (glucose-regulated protein 94) is a tumor antigen shared by many types of solid and hematological tumors [19]. Stable complexes with IgG (GRP94-IgG) are detected in the plasma of patients with gastrointestinal tumors and served as diagnostic tumor marker [19]. HSP60 upregulates the expression of MHC class II in B cells and increase the expression of CD69, CD40, and B7-2 on the surface of B cells simultaneously [20]. After HSP60 treatment, B cells activate the cytotoxicity function of T cells and promote the secretion of IL-10 and IFN-gamma inflammatory factors [21]. Hence, HSPs can promote the expression of MHCII, PDL1, and CD69 on the surface of B cells, thereby activating cytotoxic T cells.

Heat shock proteins and dendritic cells

DC cells are important antigen-presenting cells. They can bind tumor related antigens in extracellular vesicles or other special forms to DC cell surface related receptors in the tumor microenvironment. Through the opsonization of antibodies or complements and a series of enzymes, tumor related antigens are presented to T cells in the form of antigen-peptide-MHC molecular complexes. Heat stress (high-temperature treatment) can induce the release of HSP70 from tumor cells, which, in turn, activate tumor cells to produce chemokines for chemoattraction of DC and T cells via TLR4 (toll like receptor 4) signaling pathway [22]. Exosomes derived from an engineered myeloma cells carrying membrane-bound HSP70 are able to more efficiently stimulate maturation of DCs with upregulation of la(b), CD40, CD80 and inflammatory cytokines than controls after overnight incubation of immature bone-marrow derived DCs [23]. In addition, exosomes carrying HSP70 and HSP90 derived from lung cancer cell line Rab27 upregulates MHC class II, CD80 and CD86 of DCs, leading to maturation of DCs and proliferation of CD4+ T cells [24]. GP96 also mediates maturation of DCs as determined by upregulation of MHC class II and CD86 molecules [25]. Overall, HSPs are secreted from tumor cells and they can form complexes with tumor associated antigens in exosomes or other forms. For example, HSPs bind to DC cell surface receptors and upregulate related molecules such as CD80 and CD86, and finally activate T cell activity.

Heat shock proteins and macrophages

Tumor associated macrophages (TAM) in the tumor microenvironment play a crucial role in tumor migration, invasion, angiogenesis, metastasis and drug resistance. Activated M2 macrophages can suppress normal immune cells and promote tumor development. Previous studies have shown that TAM can recognize vesicles secreted by tumor cells, leading to characteristics changes in TAM [26]. Studies have shown that eHSP-72 secreted from tumor cells can promote the secretion of more macrophage inflammatory protein 2 (MIP-2) by macrophages by interacting with TLR2 (toll like receptor 2) and TLR4 on the surface of macrophages [27]. Grp94, the most represented endoplasmic reticulum-residual HSP, is a specific antigen for solid tumors and hematological tumors that is recognized by immune cells after being transferred from the endoplasmic reticulum to the cell surface. Grp94-IgG complexes in the peripheral blood of tumor patients is significantly higher than that of healthy controls. Addition of Grp94-IgG complexes to macrophage culture medium revealed enhanced differentiation of macrophages in in vivo assay [19]. HSP70, secreted from tumor cells, binds to the membrane receptor CD14 of monocytes, inducing intracellular calcium ion flow formation and upregulating the pro-inflammatory cytokine IL-1 β, IL-6 and TNF-α [28]. Macrophages were co-cultured with conditioned medium from HSP110 knock-down colorectal cancer cells HCT116 and SW480. Compared with controls, the macrophages expressed more HLA-DR receptors and secrete more TNFa and IL1b cytokines, while CD163 and CD206 were significantly reduced [29]. Similar results were observed in tumor samples of metastatic oral cancer. HSP90β secreted by tumors was recognized by TAM and promote TAM activation into M2 type [26]. In conclusion, HSPs, in the form of monomers, vesicles, or complexes, can affect macrophages’ polarization, secretion of inflammatory factors and expression of surface receptors in the tumor microenvironment.

Heat shock proteins and NK cells

NK (natural killer) cells, as the first line of defense in the human body, release cytotoxic particles through the secretion of cytokines, leading to cytotoxic effects [30]. HSP70 peptide TKD (TKDNNLLGRFELSG, aa 450-463) is the N-terminal domain of HSP70. Studies have shown that the surface receptors of NK cells, CD94/NKG2C (natural killer group 2 member C), NKG2D (Natural Killer Group 2 Member D) as well as NKp30 (natural killer receptor p30), NKp44, NKp46, and NKp80 are upregulated under the influence of HSP70 derived TKD peptide [3133]. However, HSP-bearing exosomes secreted from human hepatocellular carcinoma cells stimulate NK cells to secrete granzyme B into the tumor microenvironment [34]. Granzyme B, along with perforin, induces tumor cell apoptosis by forming transmembrane pores and cleavage of caspases [35]. HSPs efficiently stimulate NK cell cytotoxicity and granzyme B production, upregulate the expression of inhibitory receptor CD94 and downregulate the expression of activating receptors CD69, NKG2D, and NKp44 [36]. HSP70 can induce the release of granzyme B by inducing the opening of ion channels within NK cells [37]. HSP70 also activates mouse NK cells that recognize stress-inducible NKG2D ligands on tumor cells and results in a reduced tumor growth and suppression of tumor metastasis [38]. HSP70 peptide TKD was found to enhance the cytolytic activity of NK cells and NK cellsinitiated apoptosis in tumors through granzyme B release [39, 40]. Taken together, HSPs can induce cytotoxicity of NK cells by affecting surface receptors such as NKp44 and NKp46, as well as the secretion of granzyme B, thereby inhibiting tumor growth.

Heat shock proteins and MDSCs

MDSCs (myeloid-derived suppressor cells) are precursors of DCs, macrophages, and granulocytes. MDSCs are heterogeneous populations of cells that expand during cancer, inflammation and infection [41]. MDSCs are divided into two major groups: granulocyte MDSCs (CD11b+Ly6C-Ly6G+) and monocyte MDSCs (CD11b+Ly6C+Ly6G−) [42]. MDSCs can recognize HSP72- or HSP70-bearing exosomes and be activated via TLR2/MyD88 pathway or NF-κB pathway [5]. Activated MDSCs enhances Treg activity and TGF-β secretion [5]. Therefore, MDSC can recognize HSPs and signaling pathways within MDSC are activated, which in turn promote the activity of Treg cells.

Heat shock proteins and vasculature

The tumor vasculature is essential for tumor growth and survival and is a key target for anti-cancer therapy. The basic process of tumor angiogenesis is mainly caused by activation of endothelial cells under growth factor stimulation, basement membrane degradation, and recruitment of pericytes to stabilize the newly formed capillary network [43]. HSPA5 is generally highly elevated in the vasculature derived from human glioma specimens and targeting HSPA5 can sensitize the tumor vasculature to chemotherapeutic drugs, such as CPT-11, etoposide and temozolomide [44]. HSPA5, exposed on cell surfaces of proliferating endothelial cells as well as on stressed tumor cells, plays a key role in the antiangiogenic and antitumor activity of human plasminogen Kringle 5 (K5) [45]. HSP70-1 is also an angiogenic regulator. It is tightly bound to the surface of HUVECs (human umbilical vein endothelial cell) and participates in extracellular signal-related kinase (ERK)-dependent angiogenesis [46]. IL-5 as an activator of angiogenesis, promotes ERK and AKT/endothelial nitric oxide synthesis (eNOS) phosphorylation in HUVECs cells, as well as promotes microvessel sprouting from an angiogenic animal model [47]. Binding of IL-5 to IL-5Rα receptors enhances angiogenic responses by stimulating the expression of HSP70-1 via the eNOS signaling pathway [48]. In addition, HSP90 inhibitors exert anti-angiogenesis effects by affecting the PI-3K/Akt/eNOS signal transduction pathway within endothelial cells and reducing the expression of VEGFR-2 on the surface of endothelial cells. In addition, blocking the expression of HSP90 can reduce the expression and secretion of pre-angiogenic proteins derived from tumor cells, which indirectly induces the anti-angiogenic effect of tumors [48]. In summary, HSPs can bind to receptors on the surface of endothelial cells, activate the eNOS signaling pathway and promote angiogenesis in the tumor microenvironment.

Recently, HSPs have been reported to be secreted through exosomes by tumor cells. HSP-exosomes have been reported as biomarkers of cancer dissemination, response to therapy or patient prognosis [49]. A new range of functions, mostly in modulation of immune responses, have been shown for these extracellular HSPs. The understanding of the pivotal role of HSPs in tumor microenvironment and the underlying regulatory mechanisms will increase our knowledge of the etiology of cancer, as well as development of immune therapy against cancer. However, vaccines targeting HSPs are not very clinically successful, and more research is needed. This review explores interactions between HSPs and different immune cells as well as tumor vasculature in tumor microenvironment (Figure 1, Video 1). HSPs might be both targets for anticancer therapeutics and biomarkers for the monitoring of cancers. It is also an emerging target for cancer vaccines.

thumbnail Figure 1

The interactions between HSPs and different immune cells and tumor vasculature in tumor microenvironment.

Video 1

Roles of heat shock proteins intumor immune microenvironment. This video was generated by using a commercially available artificial intelligent platform Invideo AI.

Acknowledgments

We thank Professor Ming Matthew Wang at Grand Rapids Community College, Michigan, USA, for his assistance in generating the video of this article by using an artificial intelligent platform.

Funding

This study was supported by NSFC (82072604), Guangdong Basic & Applied Basic Research-Hybribio Joint Fund (2022A1515220091), Guangdong ECI Project (M202203).

Conflict of interest

The authors declare no conflict of interests.

Data availability statement

The data are available upon request.

Author contribution statement

QZ wrote the initial draft; XYG provided funding support; YL provided funding support, supervised the study and wrote the final manuscript. All authors have read and agreed the manuscript.

Ethics approval

This is a review and it does not need ethics approval.

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Cite this article as: Zhou Q, Guan X-Y, Li Y. Roles of heat shock proteins in tumor immune microenvironment. Visualized Cancer Medicine. 2024; 5, 3.

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The interactions between HSPs and different immune cells and tumor vasculature in tumor microenvironment.

In the text

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Roles of heat shock proteins intumor immune microenvironment. This video was generated by using a commercially available artificial intelligent platform Invideo AI.

In the text

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.