date: 2022-01-20T06:44:51Z pdf:unmappedUnicodeCharsPerPage: 17 pdf:PDFVersion: 1.7 pdf:docinfo:title: Transcriptional Heterogeneity and the Microbiome of Cutaneous T-Cell Lymphoma xmp:CreatorTool: LaTeX with hyperref Keywords: cutaneous T-cell lymphoma (CTCL); mycosis fungoides (MF); Sézary syndrome (SS); transcriptome; microbiome; heterogeneity access_permission:modify_annotations: true access_permission:can_print_degraded: true subject: Cutaneous T-Cell Lymphomas (CTCL) presents with substantial clinical variability and transcriptional heterogeneity. In the recent years, several studies paved the way to elucidate aetiology and pathogenesis of CTCL using sequencing methods. Several T-cell subtypes were suggested as the source of disease thereby explaining clinical and transcriptional heterogeneity of CTCL entities. Several differentially expressed pathways could explain disease progression. However, exogenous triggers in the skin microenvironment also seem to affect CTCL status. Especially Staphylococcus aureus was shown to contribute to disease progression. Only little is known about the complex microbiome patterns involved in CTCL and how microbial shifts might impact this malignancy. Nevertheless, first hints indicate that the microbiome might at least in part explain transcriptional heterogeneity and that microbial approaches could serve in diagnosis and prognosis. Shaping the microbiome could be a treatment option to maintain stable disease. Here, we review current knowledge of transcriptional heterogeneity of and microbial influences on CTCL. We discuss potential benefits of microbial applications and microbial directed therapies to aid patients with CTCL burden. dc:creator: Philipp Licht and Volker Mailänder dcterms:created: 2022-01-20T06:38:55Z Last-Modified: 2022-01-20T06:44:51Z dcterms:modified: 2022-01-20T06:44:51Z dc:format: application/pdf; version=1.7 title: Transcriptional Heterogeneity and the Microbiome of Cutaneous T-Cell Lymphoma Last-Save-Date: 2022-01-20T06:44:51Z pdf:docinfo:creator_tool: LaTeX with hyperref access_permission:fill_in_form: true pdf:docinfo:keywords: cutaneous T-cell lymphoma (CTCL); mycosis fungoides (MF); Sézary syndrome (SS); transcriptome; microbiome; heterogeneity pdf:docinfo:modified: 2022-01-20T06:44:51Z meta:save-date: 2022-01-20T06:44:51Z pdf:encrypted: false dc:title: Transcriptional Heterogeneity and the Microbiome of Cutaneous T-Cell Lymphoma modified: 2022-01-20T06:44:51Z cp:subject: Cutaneous T-Cell Lymphomas (CTCL) presents with substantial clinical variability and transcriptional heterogeneity. In the recent years, several studies paved the way to elucidate aetiology and pathogenesis of CTCL using sequencing methods. Several T-cell subtypes were suggested as the source of disease thereby explaining clinical and transcriptional heterogeneity of CTCL entities. Several differentially expressed pathways could explain disease progression. However, exogenous triggers in the skin microenvironment also seem to affect CTCL status. Especially Staphylococcus aureus was shown to contribute to disease progression. Only little is known about the complex microbiome patterns involved in CTCL and how microbial shifts might impact this malignancy. Nevertheless, first hints indicate that the microbiome might at least in part explain transcriptional heterogeneity and that microbial approaches could serve in diagnosis and prognosis. Shaping the microbiome could be a treatment option to maintain stable disease. Here, we review current knowledge of transcriptional heterogeneity of and microbial influences on CTCL. We discuss potential benefits of microbial applications and microbial directed therapies to aid patients with CTCL burden. pdf:docinfo:subject: Cutaneous T-Cell Lymphomas (CTCL) presents with substantial clinical variability and transcriptional heterogeneity. In the recent years, several studies paved the way to elucidate aetiology and pathogenesis of CTCL using sequencing methods. Several T-cell subtypes were suggested as the source of disease thereby explaining clinical and transcriptional heterogeneity of CTCL entities. Several differentially expressed pathways could explain disease progression. However, exogenous triggers in the skin microenvironment also seem to affect CTCL status. Especially Staphylococcus aureus was shown to contribute to disease progression. Only little is known about the complex microbiome patterns involved in CTCL and how microbial shifts might impact this malignancy. Nevertheless, first hints indicate that the microbiome might at least in part explain transcriptional heterogeneity and that microbial approaches could serve in diagnosis and prognosis. Shaping the microbiome could be a treatment option to maintain stable disease. Here, we review current knowledge of transcriptional heterogeneity of and microbial influences on CTCL. We discuss potential benefits of microbial applications and microbial directed therapies to aid patients with CTCL burden. Content-Type: application/pdf pdf:docinfo:creator: Philipp Licht and Volker Mailänder X-Parsed-By: org.apache.tika.parser.DefaultParser creator: Philipp Licht and Volker Mailänder meta:author: Philipp Licht and Volker Mailänder dc:subject: cutaneous T-cell lymphoma (CTCL); mycosis fungoides (MF); Sézary syndrome (SS); transcriptome; microbiome; heterogeneity meta:creation-date: 2022-01-20T06:38:55Z created: 2022-01-20T06:38:55Z access_permission:extract_for_accessibility: true access_permission:assemble_document: true xmpTPg:NPages: 18 Creation-Date: 2022-01-20T06:38:55Z pdf:charsPerPage: 3851 access_permission:extract_content: true access_permission:can_print: true meta:keyword: cutaneous T-cell lymphoma (CTCL); mycosis fungoides (MF); Sézary syndrome (SS); transcriptome; microbiome; heterogeneity Author: Philipp Licht and Volker Mailänder producer: pdfTeX-1.40.21 access_permission:can_modify: true pdf:docinfo:producer: pdfTeX-1.40.21 pdf:docinfo:created: 2022-01-20T06:38:55Z