Sestrin1, a tumor suppressor that can be rescued

ABSTRACT

SESTRIN1 is a tumor suppressor in follicular lymphoma that controls mTORC1 activity and it is inactivated by chromosomal deletions or epigenetically silenced by mutant EZH2^Y641X. Pharmacological inhibition of EZH2 promotes SESTRIN1 re-expression and it restores its tumor suppressive activity, suggesting the possibility to epigenetically control mTORC1 activity.

Follicular lymphoma (FL) is a common form of indolent B-cell malignancy characterized by numerous genomic alterations including chromosomal rearrangement, mutations, and epigenetic changes. In the context of tumor evolution, the acquisition of the chromosomal translocation t(14;18)(q32;q21), that promotes the over-expression of the anti-apoptotic protein BCL2, is an early event in FL development. Nevertheless, B-cells harboring this chromosomal re-arrangement require the accumulation of additional mutations and chromosomal copy number changes to exhibit tumorigenic capacity.^1,2 Deletions on chromosome 6q are one of the most frequent copy number alterations observed in FL patients. Tumorigenic B-cells harboring these alterations are positively selected in FL development and progression, indicating that the loss of multiple genes on chromosome 6q actively contributes to malignant B-cells transformation.³ In addition to chromosomal aberrations, several epigenetic modifiers are frequently mutated in FL, including the histone methyltransferases EZH2 and MLL2 (gene name KMT2D), the histone acetyltransferase CREBBP, and the chromatin remodeling factor ARID1A.^4,5 Epigenetic modifiers can directly and indirectly activate or repress the expression of several genes, altering the FL transcriptomic profile.⁶ Since both epigenetic changes and large chromosomal lesions simultaneously affect several genes, it is challenging from the sole analysis of genomic data to identify functionally relevant targets.

In our recent study, we used a functional genetic screen to identify new candidate tumor suppressors in FL targeted by large deletions on chromosome 6q. Through the screen analysis and the subsequent validation of the screen results in a chimeric animal model of FL, we were able to identify SESTRIN1 as a new tumor suppressor in FL.⁷ SESTRIN1 is deleted in 20% of FL lymphoma patients, most of the deletions include several genes, and in rare cases, patients harbor focal deletions, which further pinpoints to SESTRIN1 as an important target. In addition to chromosomal deletions, we found that SESTRIN1 is epigenetically silenced by the mutated protein EZH2^Y641X through increase of Histone3-Lysine-27-Methyl-3 (H3K27me3) and consequent hyper methylation of the SESTRIN1 promoter.⁷

SESTRIN1 is a member of a protein family including SESTRIN2 and SESTRIN3. These proteins are transcriptional targets of p53 (TP53, best known as p53)⁸ and they function as guanine nucleotide dissociation inhibitors regulating the activity of the Rag-A (gene name RRAGA), Rag-B (gene name RRAGB), and mTORC1 complex.⁹ In FL patients, the expression of SESTRIN2 and SESTRIN3 is not epigenetically regulated and these genes are rarely targeted by chromosomal deletions, indicating an exquisite dependency of B-cells on SESTRIN1 activity. Indeed loss of Sestrin1 is sufficient to drive lymphomagenesis in chimeric mouse model of FL.⁷

In response to genotoxic and cellular stress, p53 induces SESTRIN1 expression. Cells exposed to nutrient deprivation or DNA damage activate protective programs to block or eliminate cells that have lost their integrity. p53 is the principal controller of genome integrity and cancer cells must inactivate p53 or bypass its activity to continue to proliferate. In lymphoma genomic alterations that directly target p53 are less frequent than in other tumors, indicating that malignant B-cells in FL have acquired alternative strategies to evade p53 action. We observed that the ability of p53 to activate SESTRIN1 was significantly hampered in cells expressing mutated EZH2^Y641X. This implies that the increase of H3K27me3 on the SESTRIN1 promoter not only represses the gene expression, but it also limits the ability of p53 to bind and induce expression of SESTRIN1. As a consequence, mTORC1 activity cannot be regulated and it remains active in cells exposed to genotoxic stress.

Recent studies have highlighted the central role of mTORC1 activity to sustain FL pathogenesis. Sequencing analysis revealed mutations targeting RRAGC (best known as Rag-C) uniquely found in FL patients. Mutations in RRAGC tend to co-occur with mutations in ATP6V1B2 and ATP6AP1 genes,¹⁰ but they are mutually exclusive with SESTRIN1 deletions or epigenetic silencing.⁷ Importantly, all of these genes are important regulators of mTORC1 activity (Fig. 1). Cells harboring mutations in RRAGC are less sensitive to nutrient deprivation, and amino acid withdrawal does not reduce mTORC1 activity. Similarly, loss of SESTRIN1 contributes to sustain mTORC1 in response to DNA damage. Interestingly, the near mutual exclusivity of RRAGC and SESTRIN1 alterations suggests that one of these two alterations is sufficient to unleash mTORC1 activity and promote follicular lymphomagenesis.

Figure 1.

Several genomic lesions lead to the activation of mTORC1 signaling in Follicular Lymphoma (FL). EZH2^Y641X gain-of-function mutations occur in 18–22% of FL patients and it promotes SESTRIN1 epigenetic silencing. SESTRIN1 is also deleted in 20% of FL. These lesions are mutually exclusive with RRAGC mutations that usually occur in 8% of cases. Alterations in these genes contribute to sustain mTORC1 oncogenic activity in FL.

If Sestrin1 is silenced, it can be reawakened. If it is deleted, it cannot come back

Restoring the expression or the activity of a tumor suppressor gene is a major challenge in cancer therapy. A few years ago, we proposed to use a fusion antibody as potential therapeutic strategy to recover the activity of a soluble tumor suppressor, EPHA7³. Although this task is feasible as proof of principle, it has been arduous to translate this idea into a clinically valuable tool. Moreover, it remains unfeasible to directly re-express mutated or deleted tumor suppressors. In FL, chromosomal deletions targeting SESTRIN1 are mutually exclusive with EZH2 mutations, indicating that SESTRIN1 is epigenetically silenced but its genomic locus is intact in patients expressing the EZH2^Y641X mutated protein. Currently, several EZH2 inhibitors are being tested in clinical trials. In our study, we show that the therapeutic efficacy of these drugs is, at least in part, linked to their ability to reactivate SESTRIN1 expression. EZH2 inhibitors repress the methyltransferase enzymatic activity and are able to release the epigenetic block holding SESTRIN1 expression. Reactivation of SESTRIN1 translates in mTORC1 inhibition and decrease of protein translation, ultimately undermining tumor growth.

In summary, cells expressing mutated EZH2^Y641X are selected during the evolution of FL tumor for their ability to inhibit the expression of tumor suppressors. Indeed, while mutated EZH2 can block the expression of multiple genes, its oncogenic role is unequivocally tied with the functional relevance of its targets. Consequently, the therapeutic efficacy of EZH2 inhibitor is strictly linked to their ability to restore the activity of tumor suppressors.

Acknowledgments

This work is supported by the ISREC Foundation (E.O.), and the Swiss National Science Foundation 31003A-159637 (E.O.).

Author information

The authors declare no competing financial interests.