Gene Expression Studies in Cancer Research

A special issue of Cancers (ISSN 2072-6694). This special issue belongs to the section "Tumor Microenvironment".

Deadline for manuscript submissions: closed (31 December 2023) | Viewed by 1790

Special Issue Editor


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Guest Editor
National Cancer Institute (NCI), Bethesda, MD, USA
Interests: bioinformatics; biostatistics; genetics and genomics

Special Issue Information

Dear Colleagues,

Gene expression analyses of tissue samples are widely applied in cancer research. Tissue samples include tumors and normal tissues from cancer patients and animal models. The gene expression data are derived from tissue samples by using RNASeq, single-cell RNASeq and spatial RNASeq.  The gene expression profile of the tumors can be applied to characterize cancer subtypes to design personalized treatment plans. The RNASeq samples in different groups (subtypes or KO/KD conditions) are compared to derive differentially expressed genes that can be further applied to conduct pathway analysis and to design single and multiple gene signatures to predict patient survival, tumor metastasis and recurrence.  The recent advances in gene expression research are in these areas: cancer subtypes, using animal models to study human cancers, deconvolution of gene expression, immune therapy response prediction, gene fusion detection, alternative splicing and non-coding RNA. Other developments include the joint analysis of genotyping and gene expression (eQTL), and integrative analysis combining expression with genetic data (mutation and copy number change data) and epigenetic data. However, the results in these areas were only limited to some cancers. More research efforts are needed to expand the field for more cancer types. In this Special Issue, we will concentrate on recent research advances in these areas and best practices in gene expression analyses.

Dr. Howard H. Yang
Guest Editor

Manuscript Submission Information

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Keywords

  • gene expression
  • eQTL
  • RNASeq
  • single-cell RNASeq
  • spatial RNASeq
  • immune therapy response prediction
  • gene fusion detection

Published Papers (1 paper)

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Research

20 pages, 4148 KiB  
Article
In Silico Analysis Predicts Nuclear Factors NR2F6 and YAP1 as Mesenchymal Subtype-Specific Therapeutic Targets for Ovarian Cancer Patients
by Wanja Kassuhn, Pedro R. Cutillas, Mirjana Kessler, Jalid Sehouli, Elena I. Braicu, Nils Blüthgen and Hagen Kulbe
Cancers 2023, 15(12), 3155; https://doi.org/10.3390/cancers15123155 - 12 Jun 2023
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Abstract
Background: Tumour heterogeneity in high-grade serous ovarian cancer (HGSOC) is a proposed cause of acquired resistance to treatment and high rates of relapse. Among the four distinct molecular subtypes of HGSOC, the mesenchymal subtype (MES) has been observed with high frequency in several [...] Read more.
Background: Tumour heterogeneity in high-grade serous ovarian cancer (HGSOC) is a proposed cause of acquired resistance to treatment and high rates of relapse. Among the four distinct molecular subtypes of HGSOC, the mesenchymal subtype (MES) has been observed with high frequency in several study cohorts. Moreover, it exhibits aggressive characteristics with poor prognosis. The failure to adequately exploit such subtypes for treatment results in high mortality rates, highlighting the need for effective targeted therapeutic strategies that follow the idea of personalized medicine (PM). Methods: As a proof-of-concept, bulk and single-cell RNA data were used to characterize the distinct composition of the tumour microenvironment (TME), as well as the cell–cell communication and its effects on downstream transcription of MES. Moreover, transcription factor activity contextualized with causal inference analysis identified novel therapeutic targets with potential causal impact on transcription factor dysregulation promoting the malignant phenotype. Findings: Fibroblast and macrophage phenotypes are of utmost importance for the complex intercellular crosstalk of MES. Specifically, tumour-associated macrophages were identified as the source of interleukin 1 beta (IL1B), a signalling molecule with significant impact on downstream transcription in tumour cells. Likewise, signalling molecules tumour necrosis factor (TNF), transforming growth factor beta (TGFB1), and C-X-C motif chemokine 12 (CXCL12) were prominent drivers of downstream gene expression associated with multiple cancer hallmarks. Furthermore, several consistently hyperactivated transcription factors were identified as potential sources for treatment opportunities. Finally, causal inference analysis identified Yes-associated protein 1 (YAP1) and Nuclear Receptor Subfamily 2 Group F Member 6 (NR2F6) as novel therapeutic targets in MES, verified in an independent dataset. Interpretation: By utilizing a sophisticated bioinformatics approach, several candidates for treatment opportunities, including YAP1 and NR2F6 were identified. These candidates represent signalling regulators within the cellular network of the MES. Hence, further studies to confirm these candidates as potential targeted therapies in PM are warranted. Full article
(This article belongs to the Special Issue Gene Expression Studies in Cancer Research)
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