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Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids

One major challenge associated with lung cancer organoids (LCOs) is their predominant derivation from surgical specimens of patients with early-stage lung cancer. However, patients with advanced lung cancer, who are in need of chemotherapy, often cannot undergo surgery. Therefore, there is an urgent...

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Autores principales: Park, Dongil, Lee, Dahye, Kim, Yoonjoo, Park, Yeonhee, Lee, Yeon-Jae, Lee, Jeong Eun, Yeo, Min-Kyung, Kang, Min-Woong, Chong, Yooyoung, Han, Sung Joon, Choi, Jinwook, Park, Jong-Eun, Koh, Yongjun, Lee, Jaehyeok, Park, YongKeun, Kim, Ryul, Lee, Jeong Seok, Choi, Jimin, Lee, Sang-Hyun, Ku, Bosung, Kang, Da Hyun, Chung, Chaeuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377875/
https://www.ncbi.nlm.nih.gov/pubmed/37508518
http://dx.doi.org/10.3390/cells12141854
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author Park, Dongil
Lee, Dahye
Kim, Yoonjoo
Park, Yeonhee
Lee, Yeon-Jae
Lee, Jeong Eun
Yeo, Min-Kyung
Kang, Min-Woong
Chong, Yooyoung
Han, Sung Joon
Choi, Jinwook
Park, Jong-Eun
Koh, Yongjun
Lee, Jaehyeok
Park, YongKeun
Kim, Ryul
Lee, Jeong Seok
Choi, Jimin
Lee, Sang-Hyun
Ku, Bosung
Kang, Da Hyun
Chung, Chaeuk
author_facet Park, Dongil
Lee, Dahye
Kim, Yoonjoo
Park, Yeonhee
Lee, Yeon-Jae
Lee, Jeong Eun
Yeo, Min-Kyung
Kang, Min-Woong
Chong, Yooyoung
Han, Sung Joon
Choi, Jinwook
Park, Jong-Eun
Koh, Yongjun
Lee, Jaehyeok
Park, YongKeun
Kim, Ryul
Lee, Jeong Seok
Choi, Jimin
Lee, Sang-Hyun
Ku, Bosung
Kang, Da Hyun
Chung, Chaeuk
author_sort Park, Dongil
collection PubMed
description One major challenge associated with lung cancer organoids (LCOs) is their predominant derivation from surgical specimens of patients with early-stage lung cancer. However, patients with advanced lung cancer, who are in need of chemotherapy, often cannot undergo surgery. Therefore, there is an urgent need to successfully generate LCOs from biopsy specimens. Conventional lung biopsy techniques, such as transthoracic needle biopsy and forceps biopsy, only yield small amounts of lung tissue, resulting in a low success rate for culturing LCOs from biopsy samples. Furthermore, potential complications, like bleeding and pneumothorax, make it difficult to obtain sufficient tissue. Another critical issue is the overgrowth of normal lung cells in later passages of LCO culture, and the optimal culture conditions for LCOs are yet to be determined. To address these limitations, we attempted to create LCOs from cryobiopsy specimens obtained from patients with lung cancer (n = 113). Overall, the initial success rate of establishing LCOs from cryobiopsy samples was 40.7% (n = 46). Transbronchial cryobiopsy enables the retrieval of significantly larger amounts of lung tissue than bronchoscopic forceps biopsy. Additionally, cryobiopsy can be employed for peripheral lesions, and it is aided via radial endobronchial ultrasonography. This study significantly improved the success rate of LCO culture and demonstrated that the LCOs retained characteristics that resembled the primary tumors. Single-cell RNA sequencing confirmed high cancer cell purity in early passages of LCOs derived from patients with advanced lung cancer. Furthermore, the three-dimensional structure and intracellular components of LCOs were characterized using three-dimensional holotomography. Finally, drug screening was performed using a specialized micropillar culture system with cryobiopsy-derived LCOs. LCOs derived from cryobiopsy specimens offer a promising solution to the critical limitations of conventional LCOs. Cryobiopsy can be applied to patients with lung cancer at all stages, including those with peripheral lesions, and can provide sufficient cells for LCO generation. Therefore, we anticipate that cryobiopsy will serve as a breakthrough strategy for the clinical application of LCOs in all stages of lung cancer.
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spelling pubmed-103778752023-07-29 Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids Park, Dongil Lee, Dahye Kim, Yoonjoo Park, Yeonhee Lee, Yeon-Jae Lee, Jeong Eun Yeo, Min-Kyung Kang, Min-Woong Chong, Yooyoung Han, Sung Joon Choi, Jinwook Park, Jong-Eun Koh, Yongjun Lee, Jaehyeok Park, YongKeun Kim, Ryul Lee, Jeong Seok Choi, Jimin Lee, Sang-Hyun Ku, Bosung Kang, Da Hyun Chung, Chaeuk Cells Article One major challenge associated with lung cancer organoids (LCOs) is their predominant derivation from surgical specimens of patients with early-stage lung cancer. However, patients with advanced lung cancer, who are in need of chemotherapy, often cannot undergo surgery. Therefore, there is an urgent need to successfully generate LCOs from biopsy specimens. Conventional lung biopsy techniques, such as transthoracic needle biopsy and forceps biopsy, only yield small amounts of lung tissue, resulting in a low success rate for culturing LCOs from biopsy samples. Furthermore, potential complications, like bleeding and pneumothorax, make it difficult to obtain sufficient tissue. Another critical issue is the overgrowth of normal lung cells in later passages of LCO culture, and the optimal culture conditions for LCOs are yet to be determined. To address these limitations, we attempted to create LCOs from cryobiopsy specimens obtained from patients with lung cancer (n = 113). Overall, the initial success rate of establishing LCOs from cryobiopsy samples was 40.7% (n = 46). Transbronchial cryobiopsy enables the retrieval of significantly larger amounts of lung tissue than bronchoscopic forceps biopsy. Additionally, cryobiopsy can be employed for peripheral lesions, and it is aided via radial endobronchial ultrasonography. This study significantly improved the success rate of LCO culture and demonstrated that the LCOs retained characteristics that resembled the primary tumors. Single-cell RNA sequencing confirmed high cancer cell purity in early passages of LCOs derived from patients with advanced lung cancer. Furthermore, the three-dimensional structure and intracellular components of LCOs were characterized using three-dimensional holotomography. Finally, drug screening was performed using a specialized micropillar culture system with cryobiopsy-derived LCOs. LCOs derived from cryobiopsy specimens offer a promising solution to the critical limitations of conventional LCOs. Cryobiopsy can be applied to patients with lung cancer at all stages, including those with peripheral lesions, and can provide sufficient cells for LCO generation. Therefore, we anticipate that cryobiopsy will serve as a breakthrough strategy for the clinical application of LCOs in all stages of lung cancer. MDPI 2023-07-14 /pmc/articles/PMC10377875/ /pubmed/37508518 http://dx.doi.org/10.3390/cells12141854 Text en © 2023 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
Park, Dongil
Lee, Dahye
Kim, Yoonjoo
Park, Yeonhee
Lee, Yeon-Jae
Lee, Jeong Eun
Yeo, Min-Kyung
Kang, Min-Woong
Chong, Yooyoung
Han, Sung Joon
Choi, Jinwook
Park, Jong-Eun
Koh, Yongjun
Lee, Jaehyeok
Park, YongKeun
Kim, Ryul
Lee, Jeong Seok
Choi, Jimin
Lee, Sang-Hyun
Ku, Bosung
Kang, Da Hyun
Chung, Chaeuk
Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids
title Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids
title_full Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids
title_fullStr Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids
title_full_unstemmed Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids
title_short Cryobiopsy: A Breakthrough Strategy for Clinical Utilization of Lung Cancer Organoids
title_sort cryobiopsy: a breakthrough strategy for clinical utilization of lung cancer organoids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10377875/
https://www.ncbi.nlm.nih.gov/pubmed/37508518
http://dx.doi.org/10.3390/cells12141854
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