Degree of stemness predicts micro-environmental response and clinical outcomes of diffuse large B-cell lymphoma and identifies a potential targeted therapy
Some cells within a diffuse large B-cell lymphoma (DLBCL) have the genotype of a stem cell, the proportion of which is termed degree of stemness . We interrogated correlations between the degree of stemness with immune and stromal cell scores and clinical outcomes in persons with DLBCL. We evaluated...
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Published in | Frontiers in immunology Vol. 13; p. 1012242 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Frontiers Media S.A
08.11.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Some cells within a diffuse large B-cell lymphoma (DLBCL) have the genotype of a stem cell, the proportion of which is termed
degree of stemness
. We interrogated correlations between the
degree of stemness
with immune and stromal cell scores and clinical outcomes in persons with DLBCL. We evaluated gene expression data on 1,398 subjects from Gene Expression Omnibus to calculate the
degree of stemness
. Subjects were classified into low- and high-stemness cohorts based on restricted cubic spline plots. Weighted gene co-expression network analysis (WGCNA) was used to screen for stemness-related genes. Immune and stromal scores correlated with the
degree of stemness
(both P < 0.001). A high
degree of stemness
correlated with a shorter progression-free survival (PFS; Hazard Ratio [HR; 95% Confidence Interval [CI] =1.90 (1.37, 2.64;
P
< 0.001) and a shorter survival (HR = 2.29 (1.53, 3.44; P < 0.001).
CDC7
expression correlated with the
degree of stemness
, and CDC7-inhibitors significantly increased apoptosis (
P
< 0.01), the proportion of cells in G
1
phase (
P
< 0.01), and inhibited lymphoma growth in a mice xenograft model (
P
= 0.04). Our data indicate correlations between the
degree of stemness
, immune and stromal scores, PFS, and survival. These data will improve the prediction of therapy outcomes in DLBCL and suggest potential new therapies. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Jun Qian, Jiangsu University Affiliated People’s Hospital, China Reviewed by: Ya Zhang, Shandong Provincial Hospital Affiliated to Shandong First Medical University, China; Liang Yu, Huai’an First People’s Hospital, China These authors have contributed equally to this work This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2022.1012242 |