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Rosenquist, Richard
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Publikasjoner (10 av 239) Visa alla publikasjoner
Moysiadis, T., Baliakas, P., Rossi, D., Catherwood, M., Strefford, J. C., Delgado, J., . . . Stamatopoulos, K. (2019). Different time-dependent changes of risk for evolution in chronic lymphocytic leukemia with mutated or unmutated antigen B cell receptors [Letter to the editor]. Leukemia, 33(7), 1801-1805
Åpne denne publikasjonen i ny fane eller vindu >>Different time-dependent changes of risk for evolution in chronic lymphocytic leukemia with mutated or unmutated antigen B cell receptors
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2019 (engelsk)Inngår i: Leukemia, ISSN 0887-6924, E-ISSN 1476-5551, Vol. 33, nr 7, s. 1801-1805Artikkel i tidsskrift, Letter (Annet vitenskapelig) Published
sted, utgiver, år, opplag, sider
Nature Publishing Group, 2019
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-390327 (URN)10.1038/s41375-018-0322-7 (DOI)000473724900022 ()30679797 (PubMedID)
Forskningsfinansiär
EU, Horizon 2020, 702714EU, Horizon 2020EU, Horizon 2020Swedish Research CouncilKnut and Alice Wallenberg FoundationSwedish Cancer SocietyErik, Karin och Gösta Selanders Foundation
Tilgjengelig fra: 2019-08-09 Laget: 2019-08-09 Sist oppdatert: 2019-08-09bibliografisk kontrollert
Mundt, F., Merrien, M., Nygren, L., Sutton, L. A., Christensson, B., Wahlin, B. E., . . . Wasik, A. M. (2019). Expression of GNAZ, encoding the G alpha(z) protein, predicts survival in mantle cell lymphoma. British Journal of Haematology, 185(4), 708-712
Åpne denne publikasjonen i ny fane eller vindu >>Expression of GNAZ, encoding the G alpha(z) protein, predicts survival in mantle cell lymphoma
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2019 (engelsk)Inngår i: British Journal of Haematology, ISSN 0007-1048, E-ISSN 1365-2141, Vol. 185, nr 4, s. 708-712Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Mantle cell lymphoma (MCL), a malignancy of B-lymphocytes, has a poor prognosis. It is thus necessary to improve the understanding of the pathobiology of MCL and identify factors contributing to its aggressiveness. Our studies, based on Affymetrix data from 17 MCL biopsies, real-time quantitative polymerase chain reaction data from 18 sorted primary MCL cells and 108 MCL biopsies compared to non-malignant tissue, reveals that GNAZ expression predicts poor clinical outcome of MCL patients (Cox regression, P = 0 center dot 014) and lymphocytosis (Mann-Whitney, P = 0 center dot 011). We show that GNAZ translates to G alpha(z) protein - a signalling molecule within the G-protein coupled receptor network. Our findings suggest that GNAZ/G alpha(z) contribute to the MCL pathobiology.

sted, utgiver, år, opplag, sider
WILEY, 2019
Emneord
mantle cell lymphoma, G-protein coupled receptors, G-proteins, prognosis, lymphocytosis
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-383841 (URN)10.1111/bjh.15810 (DOI)000467276100010 ()30788840 (PubMedID)
Forskningsfinansiär
Swedish Society for Medical Research (SSMF)
Tilgjengelig fra: 2019-05-27 Laget: 2019-05-27 Sist oppdatert: 2019-05-27bibliografisk kontrollert
Chartomatsidou, E., Ntoufa, S., Kotta, K., Rovida, A., Akritidou, M. A., Belloni, D., . . . Stamatopoulos, K. (2019). Inhibition of EZH2 and immune signaling exerts synergistic antitumor effects in chronic lymphocytic leukemia. BLOOD ADVANCES, 3(12), 1891-1896
Åpne denne publikasjonen i ny fane eller vindu >>Inhibition of EZH2 and immune signaling exerts synergistic antitumor effects in chronic lymphocytic leukemia
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2019 (engelsk)Inngår i: BLOOD ADVANCES, ISSN 2473-9529, Vol. 3, nr 12, s. 1891-1896Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Key Points:

Microenvironmental stimuli affect EZH2 expression and function in CLL.Combined B-cell signaling and EZH2 inhibition showed synergistic effects on primary CLL cells.

sted, utgiver, år, opplag, sider
AMER SOC HEMATOLOGY, 2019
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-390824 (URN)10.1182/bloodadvances.2018030262 (DOI)000472782500013 ()31227476 (PubMedID)
Forskningsfinansiär
Swedish Research CouncilKnut and Alice Wallenberg Foundation
Tilgjengelig fra: 2019-08-14 Laget: 2019-08-14 Sist oppdatert: 2019-08-14bibliografisk kontrollert
Papakonstantinou, N., Ntoufa, S., Tsagiopoulou, M., Moysiadis, T., Bhoi, S., Malousi, A., . . . Stamatopoulos, K. (2019). Integrated epigenomic and transcriptomic analysis reveals TP63 as a novel player in clinically aggressive chronic lymphocytic leukemia. International Journal of Cancer, 144(11), 2695-2706
Åpne denne publikasjonen i ny fane eller vindu >>Integrated epigenomic and transcriptomic analysis reveals TP63 as a novel player in clinically aggressive chronic lymphocytic leukemia
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2019 (engelsk)Inngår i: International Journal of Cancer, ISSN 0020-7136, E-ISSN 1097-0215, Vol. 144, nr 11, s. 2695-2706Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Chronic lymphocytic leukemia (CLL) stereotyped subsets #6 and #8 include cases expressing unmutated B cell receptor immunoglobulin (BcR IG) (U-CLL). Subset #6 (IGHV1-69/IGKV3-20) is less aggressive compared to subset #8 (IGHV4-39/IGKV1(D)-39) which has the highest risk for Richter's transformation among all CLL. The underlying reasons for this divergent clinical behavior are not fully elucidated. To gain insight into this issue, here we focused on epigenomic signatures and their links with gene expression, particularly investigating genome-wide DNA methylation profiles in subsets #6 and #8 as well as other U-CLL cases not expressing stereotyped BcR IG. We found that subset #8 showed a distinctive DNA methylation profile compared to all other U-CLL cases, including subset #6. Integrated analysis of DNA methylation and gene expression revealed significant correlation for several genes, particularly highlighting a relevant role for the TP63 gene which was hypomethylated and overexpressed in subset #8. This observation was validated by quantitative PCR, which also revealed TP63 mRNA overexpression in additional nonsubset U-CLL cases. BcR stimulation had distinct effects on p63 protein expression, particularly leading to induction in subset #8, accompanied by increased CLL cell survival. This pro-survival effect was also supported by siRNA-mediated downregulation of p63 expression resulting in increased apoptosis. In conclusion, we report that DNA methylation profiles may vary even among CLL patients with similar somatic hypermutation status, supporting a compartmentalized approach to dissecting CLL biology. Furthermore, we highlight p63 as a novel prosurvival factor in CLL, thus identifying another piece of the complex puzzle of clinical aggressiveness. What's new? In chronic lymphocytic leukemia (CLL), cases with unmutated immunoglobulin receptors (U-CLL) are generally associated with inferior outcome, albeit still displaying considerable heterogeneity. Might such differences in CLL progression be explained by epigenetics? In this study, the authors found that an unusually aggressive subset of CLLs called subset #8 has a distinctive DNA-methylation profile. They also found that p63 is a novel pro-survival factor for CLL cells. These molecular studies may lead to new prognostic biomarkers, and possibly new therapeutic targets, for CLL.

Emneord
CLL, stereotypy, DNA methylation, gene expression, TP63
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-384059 (URN)10.1002/ijc.31999 (DOI)000467099500009 ()30447004 (PubMedID)
Forskningsfinansiär
EU, Horizon 2020, 644906Swedish Cancer SocietyKnut and Alice Wallenberg FoundationEU, Horizon 2020, 692298Swedish Research CouncilEU, Horizon 2020, 702714
Merknad

De 3 första författarna delar förstaförfattarskapet.

Tilgjengelig fra: 2019-06-20 Laget: 2019-06-20 Sist oppdatert: 2019-06-20bibliografisk kontrollert
Polychronidou, E., Kalamaras, I., Agathangelidis, A., Sutton, L. A., Yan, X.-J., Bikos, V., . . . Tzovaras, D. (2018). Automated shape-based clustering of 3D immunoglobulin protein structures in chronic lymphocytic leukemia. BMC Bioinformatics, 19, Article ID 414.
Åpne denne publikasjonen i ny fane eller vindu >>Automated shape-based clustering of 3D immunoglobulin protein structures in chronic lymphocytic leukemia
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2018 (engelsk)Inngår i: BMC Bioinformatics, ISSN 1471-2105, E-ISSN 1471-2105, Vol. 19, artikkel-id 414Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Background: Although the etiology of chronic lymphocytic leukemia (CLL), the most common type of adult leukemia, is still unclear, strong evidence implicates antigen involvement in disease ontogeny and evolution. Primary and 3D structure analysis has been utilised in order to discover indications of antigenic pressure. The latter has been mostly based on the 3D models of the clonotypic B cell receptor immunoglobulin (BcR IG) amino acid sequences. Therefore, their accuracy is directly dependent on the quality of the model construction algorithms and the specific methods used to compare the ensuing models. Thus far, reliable and robust methods that can group the IG 3D models based on their structural characteristics are missing. Results: Here we propose a novel method for clustering a set of proteins based on their 3D structure focusing on 3D structures of BcR IG from a large series of patients with CLL. The method combines techniques from the areas of bioinformatics, 3D object recognition and machine learning. The clustering procedure is based on the extraction of 3D descriptors, encoding various properties of the local and global geometrical structure of the proteins. The descriptors are extracted from aligned pairs of proteins. A combination of individual 3D descriptors is also used as an additional method. The comparison of the automatically generated clusters to manual annotation by experts shows an increased accuracy when using the 3D descriptors compared to plain bioinformatics-based comparison. The accuracy is increased even more when using the combination of 3D descriptors. Conclusions: The experimental results verify that the use of 3D descriptors commonly used for 3D object recognition can be effectively applied to distinguishing structural differences of proteins. The proposed approach can be applied to provide hints for the existence of structural groups in a large set of unannotated BcR IG protein files in both CLL and, by logical extension, other contexts where it is relevant to characterize BcR IG structural similarity. The method does not present any limitations in application and can be extended to other types of proteins.

Emneord
CLL protein clustering, 3D protein descriptors, descriptor fusion
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-373247 (URN)10.1186/s12859-018-2381-1 (DOI)000454362600006 ()30453883 (PubMedID)
Forskningsfinansiär
EU, Horizon 2020, 692298
Tilgjengelig fra: 2019-01-14 Laget: 2019-01-14 Sist oppdatert: 2019-01-14bibliografisk kontrollert
Wasik, A. M., Wu, C., Mansouri, L., Rosenquist, R., Pan-Hammarstrom, Q. & Sander, B. (2018). Clinical and functional impact of recurrent S1PR1 mutations in mantle cell lymphoma. BLOOD ADVANCES, 2(6), 621-625
Åpne denne publikasjonen i ny fane eller vindu >>Clinical and functional impact of recurrent S1PR1 mutations in mantle cell lymphoma
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2018 (engelsk)Inngår i: BLOOD ADVANCES, ISSN 2473-9529, Vol. 2, nr 6, s. 621-625Artikkel i tidsskrift (Fagfellevurdert) Published
sted, utgiver, år, opplag, sider
AMER SOC HEMATOLOGY, 2018
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-354348 (URN)10.1182/bloodadvances.2017014860 (DOI)000428386900004 ()29549086 (PubMedID)
Forskningsfinansiär
Swedish Research CouncilEU, European Research Council, RNAEDIT-649019Knut and Alice Wallenberg Foundation
Tilgjengelig fra: 2018-06-27 Laget: 2018-06-27 Sist oppdatert: 2018-06-27bibliografisk kontrollert
Mansouri, L., Wierzbinska, J. A., Plass, C. & Rosenquist, R. (2018). Epigenetic deregulation in chronic lymphocytic leukemia: Clinical and biological impact. Seminars in Cancer Biology, 51, 1-11
Åpne denne publikasjonen i ny fane eller vindu >>Epigenetic deregulation in chronic lymphocytic leukemia: Clinical and biological impact
2018 (engelsk)Inngår i: Seminars in Cancer Biology, ISSN 1044-579X, E-ISSN 1096-3650, Vol. 51, s. 1-11Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Deregulated transcriptional control caused by aberrant DNA methylation and/or histone modifications is a hallmark of cancer cells. In chronic lymphocytic leukemia (CLL), the most common adult leukemia, the epigenetic 'landscape' has added a new layer of complexity to our understanding of this clinically and biologically heterogeneous disease. Early studies identified aberrant DNA methylation, often based on single gene promoter analysis with both biological and clinical impact. Subsequent genome-wide profiling studies revealed differential DNA methylation between CLLs and controls and in prognostics subgroups of the disease. From these studies, it became apparent that DNA methylation in regions outside of promoters, such as enhancers, is important for the regulation of coding genes as well as for the regulation of non-coding RNAs. Although DNA methylation profiles are reportedly stable over time and in relation to therapy, a higher epigenetic heterogeneity or 'burden' is seen in more aggressive CLL subgroups, albeit as non-recurrent 'passenger' events. More recently, DNA methylation profiles in CLL analyzed in relation to differentiating normal B-cell populations revealed that the majority of the CLL epigenome reflects the epigenomes present in the cell of origin and that only a small fraction of the epigenetic alterations represents truly CLL-specific changes. Furthermore, CLL patients can be grouped into at least three clinically relevant epigenetic subgroups, potentially originating from different cells at various stages of differentiation and associated with distinct outcomes. In this review, we summarize the current understanding of the DNA methylome in CLL, the role of histone modifying enzymes, highlight insights derived from animal models and attempts made to target epigenetic regulators in CLL along with the future directions of this rapidly advancing field.

sted, utgiver, år, opplag, sider
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD, 2018
Emneord
Chronic lymphocytic leukemia, DNA methylation, Histone modification, Outcome, Prognosis
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-364003 (URN)10.1016/j.semcancer.2018.02.001 (DOI)000442066000002 ()29427646 (PubMedID)
Forskningsfinansiär
Swedish Research CouncilKnut and Alice Wallenberg FoundationSwedish Cancer SocietyThe Karolinska Institutet's Research Foundation
Tilgjengelig fra: 2018-11-05 Laget: 2018-11-05 Sist oppdatert: 2018-11-05bibliografisk kontrollert
Malcikova, J., Tausch, E., Rossi, D., Sutton, L. A., Soussi, T., Zenz, T., . . . Pospisilova, S. (2018). ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia—update on methodological approaches and results interpretation. Leukemia, 32(5), 1070-1080
Åpne denne publikasjonen i ny fane eller vindu >>ERIC recommendations for TP53 mutation analysis in chronic lymphocytic leukemia—update on methodological approaches and results interpretation
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2018 (engelsk)Inngår i: Leukemia, ISSN 0887-6924, E-ISSN 1476-5551, Vol. 32, nr 5, s. 1070-1080Artikkel, forskningsoversikt (Fagfellevurdert) Published
Abstract [en]

In chronic lymphocytic leukemia (CLL), TP53 gene defects, due to deletion of the 17p13 locus and/or mutation(s) within the TP53 gene, are associated with resistance to chemoimmunotherapy and a particularly dismal clinical outcome. On these grounds, analysis of TP53 aberrations has been incorporated into routine clinical diagnostics to improve patient stratification and optimize therapeutic decisions. The predictive implications of TP53 aberrations have increasing significance in the era of novel targeted therapies, i.e., inhibitors of B-cell receptor (BcR) signaling and anti-apoptotic BCL2 family members, owing to their efficacy in patients with TP53 defects. In this report, the TP53 Network of the European Research Initiative on Chronic Lymphocytic Leukemia (ERIC) presents updated recommendations on the methodological approaches for TP53 mutation analysis. Moreover, it provides guidance to ensure that the analysis is performed in a timely manner for all patients requiring treatment and that the data is interpreted and reported in a consistent, standardized, and accurate way. Since next-generation sequencing technologies are gaining prominence within diagnostic laboratories, this report also offers advice and recommendations for the interpretation of TP53 mutation data generated by this methodology.

sted, utgiver, år, opplag, sider
Nature Publishing Group, 2018
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-358110 (URN)10.1038/s41375-017-0007-7 (DOI)000431769800003 ()29467486 (PubMedID)
Forskningsfinansiär
EU, Horizon 2020, 692298; 644906; LQ1601German Research Foundation (DFG), SFB1074Swedish Cancer SocietySwedish Research Council, FNBr 65269705; FM MU ROZV/24/LF/2016
Tilgjengelig fra: 2018-08-24 Laget: 2018-08-24 Sist oppdatert: 2018-08-24bibliografisk kontrollert
Went, M., Sud, A., Speedy, H., Sunter, N. J., Foersti, A., Law, P. J., . . . Houlston, R. S. (2018). Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood Cancer Journal, 9, Article ID 1.
Åpne denne publikasjonen i ny fane eller vindu >>Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology
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2018 (engelsk)Inngår i: Blood Cancer Journal, ISSN 2044-5385, E-ISSN 2044-5385, Vol. 9, artikkel-id 1Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The clustering of different types of B-cell malignancies in families raises the possibility of shared aetiology. To examine this, we performed cross-trait linkage disequilibrium (LD)-score regression of multiple myeloma (MM) and chronic lymphocytic leukaemia (CLL) genome-wide association study (GWAS) data sets, totalling 11,734 cases and 29,468 controls. A significant genetic correlation between these two B-cell malignancies was shown (R-g = 0.4, P = 0.0046). Furthermore, four of the 45 known CLL risk loci were shown to associate with MM risk and five of the 23 known MM risk loci associate with CLL risk. By integrating eQTL, Hi-C and ChlP-seq data, we show that these pleiotropic risk loci are enriched for B-cell regulatory elements and implicate B-cell developmental genes. These data identify shared biological pathways influencing the development of CLL and, MM and further our understanding of the aetiological basis of these B-cell malignancies.

HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-374121 (URN)10.1038/s41408-018-0162-8 (DOI)000454815100001 ()30602759 (PubMedID)
Forskningsfinansiär
Swedish Foundation for Strategic Research , KF10-0009Knut and Alice Wallenberg Foundation, 2012.0193Swedish Research Council, 2012-1753EU, FP7, Seventh Framework Programme, LSHC-Ct-2006-037602Marianne and Marcus Wallenberg Foundation
Tilgjengelig fra: 2019-01-23 Laget: 2019-01-23 Sist oppdatert: 2019-01-23bibliografisk kontrollert
Agathangelidis, A., Ljungström, V., Scarfo, L., Fazi, C., Gounari, M., Pandzic, T., . . . Ghia, P. (2018). Highly similar genomic landscapes in monoclonal B-cell lymphocytosis and ultra-stable chronic lymphocytic leukemia with low frequency of driver mutations. Haematologica, 103(5), 865-873
Åpne denne publikasjonen i ny fane eller vindu >>Highly similar genomic landscapes in monoclonal B-cell lymphocytosis and ultra-stable chronic lymphocytic leukemia with low frequency of driver mutations
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2018 (engelsk)Inngår i: Haematologica, ISSN 0390-6078, E-ISSN 1592-8721, Vol. 103, nr 5, s. 865-873Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Despite the recent discovery of recurrent driver mutations in chronic lymphocytic leukemia, the genetic factors involved in disease onset remain largely unknown. To address this issue, we per-formed whole-genome sequencing in 11 individuals with monoclonal B-cell lymphocytosis, both of the low-count and high-count subtypes, and 5 patients with ultra-stable chronic lymphocytic leukemia (>10 years without progression from initial diagnosis). All three entities were indistinguishable at the genomic level exhibiting low genomic complexity and similar types of somatic mutations. Exonic mutations were not frequently identified in putative chronic lymphocytic leukemia driver genes in all settings, including low-count monoclonal B-cell lymphocytosis. To corroborate these findings, we also performed deep sequencing in 11 known frequently mutated genes in an extended cohort of 28 monoclonal B-cell lym phocytosis/chronic lymphocytic leukemia cases. Interestingly, shared mutations were detected between clonal B cells and paired polymorphonuclear cells, strengthening the notion that at least a fraction of somatic mutations may occur before disease onset, likely at the hematopoietic stem cell level. Finally, we identified previously unreported non-coding variants targeting pathways relevant to B-cell and chronic lymphocytic leukemia development, likely associated with the acquisition of the characteristic neoplastic phenotype typical of both monoclonal B-cell lymphocytosis and chronic lymphocytic leukemia.

HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-356089 (URN)10.3324/haematol.2017.177212 (DOI)000431396200029 ()29449433 (PubMedID)
Forskningsfinansiär
Swedish Research CouncilSwedish Cancer SocietyEU, European Research Council
Tilgjengelig fra: 2018-07-19 Laget: 2018-07-19 Sist oppdatert: 2018-07-19bibliografisk kontrollert
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