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ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion
Malignant pleural effusion (MPE) can accompany advanced lung adenocarcinoma. Recent studies suggest that MPE could contain a heterogeneous subpopulation of cells with stem-like properties, such as tumorigenicity and self-renewal, indicating that they could be the source of metastasis. Although previ...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394086/ https://www.ncbi.nlm.nih.gov/pubmed/34441397 http://dx.doi.org/10.3390/diagnostics11081463 |
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author | Kanayama, Tomohiro Taniguchi, Toshiaki Tomita, Hiroyuki Niwa, Ayumi Noguchi, Kei Matsuo, Mikiko Imaizumi, Yuko Kuroda, Takahiro Hatano, Yuichiro Okazaki, Isao Kato, Tatsuo Hara, Akira |
author_facet | Kanayama, Tomohiro Taniguchi, Toshiaki Tomita, Hiroyuki Niwa, Ayumi Noguchi, Kei Matsuo, Mikiko Imaizumi, Yuko Kuroda, Takahiro Hatano, Yuichiro Okazaki, Isao Kato, Tatsuo Hara, Akira |
author_sort | Kanayama, Tomohiro |
collection | PubMed |
description | Malignant pleural effusion (MPE) can accompany advanced lung adenocarcinoma. Recent studies suggest that MPE could contain a heterogeneous subpopulation of cells with stem-like properties, such as tumorigenicity and self-renewal, indicating that they could be the source of metastasis. Although previous studies analyzed the correlation between cancer stem cell (CSC) marker expression and clinical outcomes using lung cancer tissues, investigations regarding the association of MPE with CSC marker expression are limited. We performed immunohistochemistry to examine the expression of aldehyde dehydrogenase 1 (ALDH1) and Sal-like 4 (SALL4) in 46 cell block samples of MPE from patients with lung adenocarcinoma. ALDH1-positive and SALL4-positive cancer cells in MPE were detected in 30 (65.2%) and 21 samples (45.7%), respectively. Cluster formation was detected in 26 samples (56.5%). The number of clusters was significantly higher in ALDH1-positive/SALL4-negative samples. SALL4 expression was inversely correlated with the cluster ratio (r = −0.356) and positively associated with the Ki-67 index (r = 0.326), suggesting that MPE cells with high SALL4 expression comprised the proliferative subpopulation. In conclusion, we demonstrated that MPE contains an ALDH1-positive/SALL4-negative subpopulation exhibiting cluster formation and a SALL4-positive proliferative subpopulation. |
format | Online Article Text |
id | pubmed-8394086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83940862021-08-28 ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion Kanayama, Tomohiro Taniguchi, Toshiaki Tomita, Hiroyuki Niwa, Ayumi Noguchi, Kei Matsuo, Mikiko Imaizumi, Yuko Kuroda, Takahiro Hatano, Yuichiro Okazaki, Isao Kato, Tatsuo Hara, Akira Diagnostics (Basel) Article Malignant pleural effusion (MPE) can accompany advanced lung adenocarcinoma. Recent studies suggest that MPE could contain a heterogeneous subpopulation of cells with stem-like properties, such as tumorigenicity and self-renewal, indicating that they could be the source of metastasis. Although previous studies analyzed the correlation between cancer stem cell (CSC) marker expression and clinical outcomes using lung cancer tissues, investigations regarding the association of MPE with CSC marker expression are limited. We performed immunohistochemistry to examine the expression of aldehyde dehydrogenase 1 (ALDH1) and Sal-like 4 (SALL4) in 46 cell block samples of MPE from patients with lung adenocarcinoma. ALDH1-positive and SALL4-positive cancer cells in MPE were detected in 30 (65.2%) and 21 samples (45.7%), respectively. Cluster formation was detected in 26 samples (56.5%). The number of clusters was significantly higher in ALDH1-positive/SALL4-negative samples. SALL4 expression was inversely correlated with the cluster ratio (r = −0.356) and positively associated with the Ki-67 index (r = 0.326), suggesting that MPE cells with high SALL4 expression comprised the proliferative subpopulation. In conclusion, we demonstrated that MPE contains an ALDH1-positive/SALL4-negative subpopulation exhibiting cluster formation and a SALL4-positive proliferative subpopulation. MDPI 2021-08-12 /pmc/articles/PMC8394086/ /pubmed/34441397 http://dx.doi.org/10.3390/diagnostics11081463 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kanayama, Tomohiro Taniguchi, Toshiaki Tomita, Hiroyuki Niwa, Ayumi Noguchi, Kei Matsuo, Mikiko Imaizumi, Yuko Kuroda, Takahiro Hatano, Yuichiro Okazaki, Isao Kato, Tatsuo Hara, Akira ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion |
title | ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion |
title_full | ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion |
title_fullStr | ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion |
title_full_unstemmed | ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion |
title_short | ALDH1 and SALL4 Expression in Cell Block Samples from Patients with Lung Adenocarcinoma and Malignant Pleural Effusion |
title_sort | aldh1 and sall4 expression in cell block samples from patients with lung adenocarcinoma and malignant pleural effusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394086/ https://www.ncbi.nlm.nih.gov/pubmed/34441397 http://dx.doi.org/10.3390/diagnostics11081463 |
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