Expression and role of RIP140/NRIP1 in chronic lymphocytic leukemia

Chronic lymphocytic leukemia (CLL) is the most common form of leukemia in Western countries and mainly affects elderly individuals. CLL is characterized by the accumulation of malignant mature B cells in bone marrow, blood and lymphoid tissues. The clinical course of CLL is extremely heterogeneous, with many patients presenting an indolent disease, whereas others exhibit an aggressive pathology and require treatment [1,2].

The diagnosis of CLL is based on biological criteria including the presence of a chronic lymphocytosis (≥5.10⁹/L) with a typical phenotype characterized by a κ or λ light chain restriction, the co-expression of B cell markers (CD19, CD20, CD22 with a low density, CD23) with the CD5 antigen (in the absence of other pan-T cell markers) and the expression of additional markers like CD200 or CD43 [3]. These characteristics are also sufficient for the distinction between CLL and other mature B cell disorders such as prolymphocytic leukemia, hairy-cell leukemia, mantle-cell lymphoma, or other lymphomas that can mimic CLL.

CLL has previously been considered as a single entity with a variable clinical course. Recently, there has been considerable progress in the identification of molecular and cellular markers that may predict disease progression in patients with CLL [2]. Particularly, mutational profiles of Ig genes and cytogenetic abnormalities have been demonstrated to display a strong prognostic value (see below).

The transcription cofactor RIP140 (receptor-interacting protein of 140 kDa), known as nuclear receptor-interacting protein 1 (NRIP1), was first identified in human breast cancer cells through its interaction with the estrogen receptor α [4]. RIP140 was also shown to interact with many other nuclear receptors and transcription factors (for a review see [5]). RIP140 mainly acts as a transcriptional repressor by means of four inhibitory domains (see Figure 1) that recruit histone deacetylases or C-terminal binding proteins [6,7]. Moreover, several post-translational modifications, such as sumoylation and acetylation, play important roles in controlling the subcellular location and repressive activity of RIP140 (for a review [8]). RIP140 is an ubiquitously expressed gene, located on chromosome 21 in humans, whose transcription is finely regulated at the transcriptional level [9,10]. The RIP140 gene exhibits two promoters and several exons, the last one encompassing the whole coding sequence (see Figure 1).

The physiological importance of RIP140 has been evaluated using mice devoid of the RIP140 gene (RIPKO mice). These animals are viable but display a wide range of phenotypic alterations in various tissues and organs, such as infertility of female mice [11] or reduced body fat content [12]. A more recent work demonstrated that they suffer severe cognitive impairments [13]. Besides these important physiological roles, RIP140 has recently been shown to regulate key oncogenic signaling pathways that impact cancer initiation and progression [14-16].

Hematopoietic stem cells (HSCs) are rare and multipotent, self-renewing precursor cells which are able to generate all specialized cells of the blood system [17]. A precise regulation of HSC proliferation and cell fate decisions is necessary to maintain ongoing production of mature blood cells throughout adult life and for rapid, regenerative responses to hematologic injury. Several studies indicated the importance of active maintenance of HSC stem cell function and identified genes that perturb HSC quiescence and disrupt stem cell maintenance and homeostatic blood cell production [18,19]. Many of these genes encode transcription factors or cell cycle regulators that directly modulate the proliferative activity of HSC.

By using gene expression microarray and systems biology tools, a functional network reconstruction was performed in cord blood CD133+ HSCs in order to identify genes involved in stemness [20]. The RIP140 gene was found highly expressed in HSC, as well as in mesenchymal and neural stem cells. Another study identified the RIP140 gene as being downregulated in mobilized HSC compared to HSC at steady-state [21]. The same report described a decrease in RIP140 expression in leukemic HSC obtained from the bone marrow of Jun B-deficient mice (a model of chronic myelogenous leukemia) as compared to HSC from wild-type mice. Altogether, these data suggested that RIP140 might be an important factor required for the maintenance and function of normal quiescent HSC. Concerning its expression in the different hematopoietic cellular types, a study reported a low RIP140 gene expression in T cells and the highest expression level in NK cells [22] (see Table 1).

Genetic aberrations such as recurrent losses or gains of chromosomal material as well as mutations of key tumor suppressors have been identified in CLL. Approximately 80% of CLL cases exhibit aberrations in a few recurrently affected chromosomal regions. These aberrations are important “drivers” of the disease and are also considered as prognosis biomarkers. CLL has turned out to be a multifaceted disease with pathogenic mechanisms including genetic aberrations, antigen processing, and microenvironmental interactions. As a consequence, there is a remarkable heterogeneity in the clinical course among patient subgroups with distinct genetic features.

According to the mutation status of immunoglobulin heavy chain variable gene segments (IGHVs), CLL patients can be classified in two groups displaying a very different clinical course [23]. Patients with an unmutated IGHV genetic profile show an unfavorable evolution, whereas patients with mutated IGHV have a better prognosis. Other poor prognostic markers in CLL are the chromosomal deletion at 11q (TP53 locus) or 17p (ATM locus). Concerning patients with del(11q), the poor outcome of is overcome by chemoimmunotherapy with fludarabine, cyclophosphamide, rituximab (FCR) [2]. More recently, recurrent mutations of NOTCH1, SF3B1, and TP53 have been shown to be associated with an adverse prognostic impact in CLL [24]. With the development of microarray technology and transcriptomic analyses, additional markers such as zeta-associated protein 70 (ZAP70), lipoprotein lipase (LPL), CLL upregulated 1 (CLLU1), transcription factor 7 (TCF7), T cell leukemias/lymphoma (TCL1A), or a disintegrin and metalloprotease domain 29 (ADAM29) have been characterized [25,26].

RIP140 was first identified as a CLL prognostic factor in a gene expression-based study using a cohort of 130 patients [22]. Furthermore, the RIP140 gene was shown as being part of a recently reported eight-gene expression signature which defined a risk score for CLL patients [27]. Low expression of RIP140 is associated with poor prognostic value for overall survival (OS) and time to treatment requirement (Figure 2). Although no studies have exclusively been focused on RIP140 in CLL, several other published data reported the deregulation of RIP140 gene expression in this pathology (Table 2). Many of these studies showed its differential expression with regard to IGHV mutational status [28-30]. In the study of van’t Veer et al., it was observed that deletion 17p13, associated with short treatment-free intervals, was more frequent in RIP140 negative cases. Similarly, deletion 11q22, which is accepted as an indicator of unfavorable prognosis [31], was only seen in RIP140 negative cases [22]. More recently, some of us reported a new gene expression-based risk score in CLL specimens corresponding to 20 genes (22 probe sets), whose expression splits patients of two independent cohorts into two risk categories [32]. Interestingly, the RIP140 expression kept prognostic value in multivariate COX analysis leading to a new risk stratification of patients with CLL.

Finally, emerging evidence indicates that the stromal tumor microenvironment plays important roles in the pathogenesis and progression of CLL. The expression of stromal-associated genes has been evaluated using gene expression profiling [33]. Interestingly, the NRIP1 gene was found to be underexpressed in cells isolated from peripheral blood, bone marrow, and lymph nodes from CLL patients in comparison with healthy donors.

Since its identification as an estrogen receptor binding protein [4], RIP140 has been characterized as a partner for many transcription factors involved in major oncogenic signaling pathways (Figure 1). Although no published studies support that RIP140 alters the biology of CLL, some of the pathways targeted by RIP140 are highly relevant in CLL biology.

Few studies have analyzed the deregulation of the RIP140 gene expression in other hematological diseases. RIP140 expression has been found to be significantly upregulated in acute myeloid leukemia (AML) with complex karyotypes and abnormal chromosome 21 [52]. By contrast, RIP140 levels are decreased in acute promyelocytic leukemia (APL), a subtype of AML most commonly characterized by the fusion of the retinoic acid receptor α gene to the promyelocytic leukemia (PML) gene [53,54].

The NRIP1 gene has also been involved in genomic translocations. Array comparative genomic hybridization analysis performed on a patient diagnosed with a precursor B cell acute lymphocytic leukemia (ALL) with the t(9;22) translocation, identified the NRIP1 gene as being interrupted at the breakpoints of 21q21.1, and joined with the UHRF1 gene at 19p13.3 as a possible fusion gene, 5′-NRIP1/UHRF1-3′ on the derivative chromosome 19 [55]. Another paper described a breakpoint of t(3;21) (q26;q11) that was assigned to be within the EVI1 and NRIP1 gene and generate a putative NRIP1-EVI1 fusion protein [56]. Finally, another fusion event involving the NRIP1 gene was reported with the open reading frame C21orf34 (also at 21q21 approximately 1 MB apart) in a patient with chronic myelomonocytic leukemia [57]. The fusion took place just upstream of miR-125b-2 and was validated by capillary sequencing. Altogether, these data suggest that the NRIP1 gene could be involved in the pathogenesis of different types of leukemia.

Data clearly suggest that a high expression of RIP140 is a favorable prognostic marker in CLL. However, further work is needed to demonstrate that RIP140 alters CLL biology and to define precisely which signaling pathways are critically regulated by this transcription factor and account for its prognostic value. Several nuclear signaling pathways, including Wnt and NF-κB, are known to be regulated by RIP140 and could be good candidates. In addition, cell models for CLL [58,59] and other types of leukemia [60] have been established and will be useful to define the role of RIP140 at the cellular level. Finally, the use of mouse models with loss and gain of function will be valuable to decipher the role of this gene in normal and tumoral HSC biology.