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 |
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08.11.2022
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Abstract | 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. |
---|---|
AbstractList | 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. 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 G1 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.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 G1 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. 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 G1 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. |
Author | Gale, Robert Peter Hu, Fang Song, Yuanbin Liang, Yang Li, Huan Chen, Shuiqin Li, Lei |
AuthorAffiliation | 3 Department of ICU, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center , Guangzhou , China 4 Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Medical Research Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University , Guangzhou , China 5 Haematology Research Centre, Department of Immunology and Inflammation, Haematology Research Centre, Imperial College London , London , United Kingdom 2 Department of Hematologic Oncology, Sun Yat-sen University Cancer Center , Guangzhou , China 1 Sate Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center for Cancer Medicine , Guangzhou , China |
AuthorAffiliation_xml | – name: 1 Sate Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Collaborative Innovation Center for Cancer Medicine , Guangzhou , China – name: 2 Department of Hematologic Oncology, Sun Yat-sen University Cancer Center , Guangzhou , China – name: 3 Department of ICU, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center , Guangzhou , China – name: 5 Haematology Research Centre, Department of Immunology and Inflammation, Haematology Research Centre, Imperial College London , London , United Kingdom – name: 4 Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Medical Research Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University , Guangzhou , China |
Author_xml | – sequence: 1 givenname: Fang surname: Hu fullname: Hu, Fang – sequence: 2 givenname: Huan surname: Li fullname: Li, Huan – sequence: 3 givenname: Lei surname: Li fullname: Li, Lei – sequence: 4 givenname: Robert Peter surname: Gale fullname: Gale, Robert Peter – sequence: 5 givenname: Yuanbin surname: Song fullname: Song, Yuanbin – sequence: 6 givenname: Shuiqin surname: Chen fullname: Chen, Shuiqin – sequence: 7 givenname: Yang surname: Liang fullname: Liang, Yang |
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CitedBy_id | crossref_primary_10_1038_s41392_024_01851_y |
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Copyright | Copyright © 2022 Hu, Li, Li, Gale, Song, Chen and Liang. Copyright © 2022 Hu, Li, Li, Gale, Song, Chen and Liang 2022 Hu, Li, Li, Gale, Song, Chen and Liang |
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Notes | 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 |
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Snippet | 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... 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... |
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StartPage | 1012242 |
SubjectTerms | dequalinium chloride diffuse large B-cell lymphoma Immunology single-sample gene set enrichment analysis stem cells targeted therapy weighted gene co-expression network analysis |
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Title | Degree of stemness predicts micro-environmental response and clinical outcomes of diffuse large B-cell lymphoma and identifies a potential targeted therapy |
URI | https://www.proquest.com/docview/2740512112 https://pubmed.ncbi.nlm.nih.gov/PMC9678919 https://doaj.org/article/7efbf16e087f4612a96cf2c90f20e354 |
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