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Clinical and biological relevance of the transcriptomic-based prostate cancer metastasis subtypes MetA-C
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Patologi.
Umeå universitet, Medicinska fakulteten, Institutionen för strålningsvetenskaper, Onkologi.
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Patologi.ORCID-id: 0000-0001-5394-7239
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Patologi.ORCID-id: 0009-0002-0666-8952
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2022 (Engelska)Ingår i: Molecular Oncology, ISSN 1574-7891, E-ISSN 1878-0261, nr 4Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

To improve treatment of metastatic prostate cancer, the biology of metastases needs to be understood. We recently described three subtypes of prostate cancer bone metastases (MetA-C), based on differential gene expression. The aim of this study was to verify the clinical relevance of these subtypes, and to explore their biology and relations to genetic drivers. Freshly-frozen metastasis samples were obtained as hormone-naive (n=17), short-term castrated (n=21) or castration resistant (n=65) from a total of 67 patients. Previously published sequencing data from 573 metastasis samples was also analyzed. Through transcriptome profiling and sample classification based on a set of predefined MetA-C-differentiating genes, we found that most metastases were heterogeneous for the MetA-C subtypes. Overall, MetA was the most common subtype, while MetB was significantly enriched in castration-resistant samples and in liver metastases, and consistently associated with poor prognosis. By gene set enrichment analysis, the phenotype of MetA was described by high androgen response, protein secretion and adipogenesis, MetB by high cell cycle activity and DNA repair, and MetC by epithelial-to-mesenchymal transition and inflammation. The MetB subtype demonstrated single-nucleotide variants of RB transcriptional corepressor 1 (RB1) and loss of 21 genes at chromosome 13, including RB1, but provided independent prognostic value to those genetic aberrations. In conclusion, a distinct set of gene transcripts can be used to classify prostate cancer metastases into the subtypes MetA-C. The MetA-C subtypes show diverse biology, organ tropism and prognosis. The MetA-C classification may be used independently, or in combination with genetic markers, primarily to identify MetB patients in need of complementary therapy to conventional androgen-receptor-targeting treatments.

Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2022. nr 4
Nyckelord [en]
MetA-C, Metastasis, Prognosis, Prostate cancer, Subtypes, Transcriptomic
Nationell ämneskategori
Cancer och onkologi
Identifikatorer
URN: urn:nbn:se:umu:diva-190463DOI: 10.1002/1878-0261.13158ISI: 000734478400001PubMedID: 34889043Scopus ID: 2-s2.0-85121666619OAI: oai:DiVA.org:umu-190463DiVA, id: diva2:1620607
Tillgänglig från: 2021-12-16 Skapad: 2021-12-16 Senast uppdaterad: 2023-10-23Bibliografiskt granskad
Ingår i avhandling
1. MicroRNA expression profiles in prostate cancer bone metastases: functional effects of microRNA-23c, -375, and -4328
Öppna denna publikation i ny flik eller fönster >>MicroRNA expression profiles in prostate cancer bone metastases: functional effects of microRNA-23c, -375, and -4328
2023 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Non-coding microRNAs (miRNAs) function as post-transcriptional regulators of gene expression by interacting with messenger RNA. Dysregulation of miRNAs has many possible consequences, including tumor-suppressive or -promoting ones, and restoring or preventing the effects of miRNA alteration has therapeutic potential.

Metastatic prostate cancer (PC) spreads to the bone and is treated with castration therapy. Eventually, metastases relapse into castration-resistant PC (CRPC) growth. Recently, our laboratory described metastatic PC subtypes, termed MetA-C, defined based on transcriptomic differences and linked to different morphology and prognosis. Patients with MetB metastases have particularly poor prognosis.

The overall aim of the thesis was to identify novel biomarkers and therapeutic targets for metastatic PC, with a focus on miRNAs. The specific aims were to: (1) identify miRNAs associated with PC progression into bone metastasis, and their functional roles; (2) verify the MetA-C subtypes, their prognostic importance, and their relation to genetic profiles in independent validation cohorts; (3) explore miRNA expression profiles of PC bone metastases, specifically in relation to the MetA-C subtypes, and whether specific miRNAs show potential to inhibit the aggressive MetB subtype.

Study 1: Differentially expressed miRNAs (n=79) were identified by microarray analysis by comparing miRNA levels in bone metastatic (n=14) or localized PC (n=7) samples to benign samples (n=7). Downregulation of miRNA-23c and -4328 was verified by qRT-PCR analysis, including a larger cohort of bone metastases (n=67).  Overexpression of miRNA-23c or -4328 in PC cells resulted in attenuated cell growth in vitro. High levels of miRNA-23c were detected in extracellular vesicles shed from overexpressing cells. Overexpression of miRNA-23c did not obviously affect tumor growth or angiogenesis in vivo.  

Study 2: The existence and prognostic value of the MetA-C subtypes was verified by transcriptomic analysis of bone metastasis samples (n=103), and by subtyping publicly available data from metastatic samples (n=573) from external patient cohorts. The MetB subtype was associated with high tumor-cell proliferation, low androgen receptor activity, and poor prognosis in all cohorts, and provided independent prognostic information in addition to genetic aberrations.

Study 3: The miRNA profiles of 96 bone metastasis samples from Study 2 were examined using microarray analysis. Four sample clusters not obviously related to the MetA-C subtypes were observed. Expression levels of miRNA-375, however, were inversely related to MetB. MiRNA-375 overexpression in C4-2B resulted in a cellular switch of subtype, from being dominant MetB to dominant MetA. In parallel, reduced cell growth and signs of increased cell adhesion were observed.

In conclusion, altered miRNA profiles may contribute to progression of PC into bone metastasis, and to the development of different metastasis subtypes. The MetB subtype is associated with poor prognosis and low expression of miRNA-375. Therapy stratification based on the MetA-C subtypes should be considered in the future. Restoration of miRNA-375 in MetB tumors may offer a novel treatment option.

Ort, förlag, år, upplaga, sidor
Umeå: Umeå University, 2023. s. 76
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 2269
Nyckelord
Prostate cancer bone metastases, microRNA, metastatic subtypes, extracellular vesicles
Nationell ämneskategori
Cancer och onkologi
Forskningsämne
patologi
Identifikatorer
urn:nbn:se:umu:diva-215629 (URN)978-91-8070-168-6 (ISBN)978-91-8070-169-3 (ISBN)
Disputation
2023-11-17, Hörsal B, byggnad 1D, 9 tr, Tandläkarhögskolan, Norrlands Universitetssjukhus, Umeå, 13:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2023-10-27 Skapad: 2023-10-23 Senast uppdaterad: 2023-10-23Bibliografiskt granskad

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Thysell, ElinKöhn, LindaSemenas, JuliusJäremo, HelenaLundholm, MarieThellenberg-Karlsson, CamillaWidmark, AndersCrnalic, SeadJosefsson, AndreasNilsson, R. Jonas A.Bergh, AndersWikström, Pernilla

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Thysell, ElinKöhn, LindaSemenas, JuliusJäremo, HelenaLundholm, MarieThellenberg-Karlsson, CamillaWidmark, AndersCrnalic, SeadJosefsson, AndreasNilsson, R. Jonas A.Bergh, AndersWikström, Pernilla
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