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Oncotarget. 2010 October; 1(6): 457–460.
Published online 2010 October 1.
PMCID: PMC3069685
NIHMSID: NIHMS240847

An Activating Transcription Factor 5-Mediated Survival Pathway as a Target for Cancer Therapy

Abstract

Genes that are highly expressed in cancer cells and are essential for their viability are attractive targets for the development of novel cancer therapeutics. Activating transcription factor 5 (ATF5) is an anti-apoptotic protein that is highly expressed in malignant glioma but not normal brain tissues, and is essential for glioma cell survival. Recent work has revealed an essential survival pathway mediated by ATF5 in malignant glioma; pharmacological inhibition of this pathway leads to tumor regression in mice. ATF5 is also highly expressed in a variety of other cancers, and preliminary studies have shown that the ATF5-mediated survival pathway is active in diverse human cancer cell lines. Targeting this pathway may therefore have therapeutic implications for the treatment of a wide range of cancers. In this perspective, we summarize recent advances in ATF5 research, focusing on its role in promoting cancer and its potential as a target for cancer therapy.

Keywords: ATF5, anti-apoptosis, cancer therapy, malignant glioma, survival pathway

INTRODUCTION

The mammalian activating transcription factor/cyclic AMP responsive element-binding (ATF/CREB) family of transcription factors comprises a large group of proteins whose members have diverse roles in development, differentiation, cellular proliferation and apoptosis. Members of the ATF/CREB family contain related basic leucine zipper (bZIP) domains; the basic region is enriched with lysine and arginine residues and is involved in DNA binding, whereas the leucine zipper motif mediates protein-protein interactions. ATF/CREB proteins bind as homo- or hetero-dimers to a DNA-binding site known as the cyclic AMP responsive element (CRE), which has the consensus sequence TGACGTCA (reviewed in [1]).

ATF5, previously designated as ATFx (or ATF7 in mice), was first isolated as a binding partner of granulocyte colony-stimulating factor (G-CSF) gene promoter element 1-binding protein (GPE1-BP), a protein involved in regulating G-CSF expression [2]. Subsequent studies have revealed that ATF5 can either homodimerize or form heterodimers with ATF4 or CCAAT enhancer-binding protein (C/EBP), and bind CRE elements [3,4] or a recently-identified novel DNA motif with the consensus sequence C(C/T)TCT(T/C)CCTTA [5]. ATF5 has also been shown to heterodimerize with the human T-cell leukemia virus type 1 (HTLV-1) Tax transactivator protein and bind to the Tax-responsive element, a member of the asymmetric CRE family of enhancer sequences [6].

A role for ATF5 in promoting cell survival was first suggested from gene expression profiling analysis in murine pro-B lymphocytic cells induced to undergo apoptosis following withdrawal of the cytokine interleukin-3 (IL-3) [7]. Among the most dramatic changes observed was a large decrease in ATF5 expression, raising the possibility that ATF5 had a role in cell survival. Subsequent work revealed that ATF5 plays a critical role in antagonizing apoptosis induced by either the deprivation of IL-3 or the expression of a pro-apoptotic protein 24p3 in murine pro-B lymphocytes, or by growth factor withdrawal in HeLa cells [8].

ATF5 EXPRESSION IN CANCER

In cancer cells, genes that induce apoptosis are often inactivated or down-regulated, whereas anti-apoptotic genes are frequently activated or over-expressed. Consistent with this paradigm, a number of studies have demonstrated that ATF5 is highly expressed in a variety of cancer cell types, whereas it is not detectably expressed in most normal human tissues (the exceptions being the liver, prostate and testis, where ATF5 is expressed at a high level [6,9]). For example, a comparison of ATF5 protein levels between normal and neoplastic samples using tissue microarrays revealed that in all malignant tissues examined—including those of the prostate, colon, endometrium, breast, ovary, pancreas, gastric, and lung—the percentage of ATF5-positive cells is significantly higher than that in normal tissues [10]. Similarly, a query of the Oncomine cancer profiling database revealed that, in general, the expression level of ATF5 is significantly higher in malignant tissues than their normal counterpart tissues [11]. The only exception appears to be hepatocellular carcinoma cells, which express lower levels of ATF5 than normal liver cells; this discrepancy may be due to epigenetic silencing of ATF5 in hepatocellular carcinoma cells through promoter methylation [12]. Notably, increased levels of ATF5 have been observed in primary brain tumors, and ATF5 expression is particularly high in glioblastoma, an aggressive form of malignant glioma [10,11].

A pair of studies has provided intriguing evidence that high ATF5 expression levels may correlate with poor prognosis in cancer patients. In one study, a retrospective analysis of 23 individuals with glioblastoma revealed that patients harboring tumors expressing high levels of ATF5 had substantially shorter survival times than those with tumors in which ATF5 expression was low or undetectable [11]. In another study, expression profiling in chronic lymphocytic leukemia (CLL) patients of known clinical outcome identified ATF5 as a gene whose significant over-expression correlates with poor patient outcome [13].

IDENTIFICATION OF AN ESSENTIAL ATF5-MEDIATED SURVIVAL PATHWAY IN MALIGNANT GLIOMA: THERAPEUTIC IMPLICATIONS

Inhibition of ATF5 activity, using a dominant negative form of ATF5, kills human and rat glioblastoma cells but does not affect normal cells surrounding the tumor, indicating ATF5 is selectively essential for the survival of glioblastoma cells [10]. The high expression of ATF5 in brain tumors, combined with the fact that it is selectively essential for glioma cell survival, make ATF5 an appealing potential therapeutic target for the treatment of malignant glioma. However, developing effective small-molecular inhibitors of transcription factors has proven to be challenging [14].

To uncover the upstream signaling pathways that control the expression and activity of ATF5—with the goal of identifying more targetable proteins, such as kinases, required for glioma cell survival—we performed a genome-wide RNA interference (RNAi) screen for factors that are required for transcription of the ATF5 gene [11]. Because loss of ATF5 function within a cell would induce apoptosis, and therefore preclude the subsequent identification of candidate short hairpin RNAs (shRNAs), we developed a novel negative-selection strategy (Figure (Figure1).1). This strategy was based on the ability of diphtheria toxin (DT) to kill cells that express the DT receptor (DTR). Mouse cells lack a functional DTR and are DT resistant [15]. We generated a mouse malignant glioma GL261 cell line stably expressing the human DTR driven by the mouse ATF5 promoter; the ATF5 promoter is normally active in GL261 cells, which drives expression of the DTR gene and confers susceptibility to DT. We then used this stable cell line to screen for shRNAs that could inactivate the ATF5 promoter and, consequently, give rise to a DT-resistant clone. Because these shRNAs would also inhibit expression of the endogenous ATF5 gene and induce apoptosis, the cell line was kept alive by the expression of ATF5 driven by a constitutive promoter. DT-resistant clones were isolated, and positive shRNAs were identified and then validated for their ability to inhibit expression of the endogenous ATF5 gene.

Figure 1
Schematic summary of the genome-wide RNAi negative-selection screen used to identify factors required for transcription of ATF5

This approach identified 12 genes as regulators of ATF5 expression, and further analyses revealed the upstream signaling pathways that regulate ATF5 expression in malignant glioma (summarized in Figure Figure2).2). Cell surface receptors (e.g. fibroblast growth factor receptor (FGFR) or epidermal growth factor receptor (EGFR)) activate downstream RAS/mitogen-activated protein kinase (RAS/MAPK) or phosphoinositide-3-kinase (PI3K) signaling pathways through FGFR substrate 2 (FRS2) and culminate in the activation of CREB protein 3-like 2 (CREB3L2), which in turn stimulates transcription of ATF5. ATF5 then antagonizes apoptosis by directly up-regulating expression of myeloid cell leukemia sequence 1 (MCL1), an anti-apoptotic B-cell leukemia/lymphoma 2 (BCL2) family member.

Figure 2
An essential ATF5-mediated survival pathway in malignant glioma

Pharmacological inhibitors of several components of that ATF5-mediated survival pathway are commercially available (see Figure Figure2).2). One of these inhibitors, sorafenib, is a multi-kinase inhibitor whose strongest activity is against RAF kinases and has been used to treat several different types of cancers [16,17]. Sorafenib inhibits the growth of human malignant glioma xenografts in mice, which suggests it may also be used to treat malignant glioma [11]. Furthermore, sorafenib sensitizes human malignant glioma xenografts to temozolomide, a chemotherapeutic agent commonly used to treat malignant glioma [18]. Inhibition of other components of the ATF5-mediated survival pathway, including FGFR (using the specific inhibitor PD173074), EGFR (CL-387,785), RAS (manumycin A), MEK (U0126), ERK (FR180204) and PI3K (LY294002), also induces apoptosis in malignant glioma cells [11]. Further investigation will verify whether these inhibitors may also be used to treat malignant glioma.

In addition to glioblastoma, ATF5 is also essential for the viability of other cancer cell types. For example, inhibition of ATF5 by a dominant negative mutant selectively kills breast cancer cells but not normal breast epithelial cells [10]. Furthermore, RNAi-mediated knockdown of ATF5 induces apoptosis in a variety of tumor cell lines derived from lung, prostate, skin, and ovary [11]. Taken together these studies demonstrate that ATF5 mediates cell survival in many cancers, and suggest that inhibition of the ATF5-mediated survival pathway may have therapeutic implications for the treatment of a wide range of malignancies.

FUTURE DIRECTIONS

Further investigations will reveal whether the ATF5-mediated survival pathway represents an efficacious target for the treatment of cancers in addition to glioblastoma. Likewise, given that ATF5 is aberrantly over-expressed in many tumor types, it would be interesting to investigate whether high ATF5 expression is generally linked to poor prognosis of cancer patients, as has been observed in glioblastoma and CLL.

Mechanistically, a further understanding of the physiological and pathological role of ATF5 in vivo would greatly benefit from the generation of ATF5 knock-out mice. If homozygous deletion of the ATF5 gene does not result in embryonic lethality, then crossing ATF5 knock-out mice with mice bearing genetic mutations that induce tumorigenesis would ascertain whether ATF5 is essential for tumor formation and progression in vivo.

It is possible that ATF5 antagonizes apoptosis through multiple targets in addition to MCL1. For example, ATF5 has been shown to promote cell survival through transcriptional activation of heat shock protein 27 (Hsp27) in rat H9c2 cells [19]. Chromatin immunoprecipitation coupled with deep sequencing (ChIP-seq) could be used to identify ATF5 target genes and study ATF5 function on a genome-wide level. Identification of additional ATF5 target genes would further define the important role of ATF5 in cancer development, and may also identify additional potential therapeutic targets.

Finally, it is worth noting that the genome-wide RNAi negative-selection screening approach used to identify components of the ATF5-mediated survival pathway represents a general strategy that can be applied to identify essential survival pathways in other types of cancer cells. Such studies may reveal new regulatory pathways that contribute to malignant transformation and are potential therapeutic targets.

Acknowledgments

This work is supported by National Institutes of Health grant R01CA115817 to M.R.G. M.R.G is an investigator of the Howard Hughes Medical Institute.

Footnotes

The authors declared no potential conflicts of interest with respect to the authorship and/or publication of this article.

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