Home LiteratureArticle Details
PMID: 2386953 Published · ppublish English Journal Article

Peripheral airway cell differentiation in human lung cancer cell lines.

Cancer research ·Vol. 50 ·No. 17 ·1990-09-01 ·Pages 5481-7

Gazdar AF, Linnoila RI, Kurita Y, Oie HK, Mulshine JL, Clark JC, Whitsett JA

Abstract

Clara cells and type II pneumocytes are the progenitor cells of the bronchioles and alveoli, respectively. These peripheral airway cells (PAC) contain characteristic cytoplasmic structures and express surfactant associated proteins. PAC cell markers are expressed by many pulmonary adenocarcinomas having papillary and/or lepidic growth patterns, which are characteristics of the bronchioloalveolar and papillary subtypes. We investigated the expression of PAC markers in a panel of 41 lung cancer cell lines. Ultrastructural studies demonstrated the presence of cytoplasmic structures characteristic of Clara cells or of type II pneumocytes in 9 of 34 (26%) non-small cell lung cancer cell lines, including 7 of 17 (41%) adenocarcinomas, one squamous cell carcinoma, and one large cell carcinoma. Of interest, the cytoplasmic structures were present in 5 of 6 (83%) cell lines initiated from papillolepidic adenocarcinomas. In addition, we examined the lines for expression of the surfactant associated proteins SP-A, SP-B, and SP-C. Eight of the nine cell lines containing cytoplasmic inclusions characteristic of PAC cells also expressed protein and/or RNA of SP-A, the major surfactant associated protein. Five of these lines expressed SP-B RNA (either constitutively or after dexamethasone induction), while a single line expressed SP-C only after dexamethasone induction. None of six small cell lung cancer cell lines examined expressed any of the PAC markers. Thus, PAC markers are expressed frequently (but not exclusively) in pulmonary adenocarcinoma cell lines, especially in those initiated from tumors having papillolepidic growth patterns. The establishment and identification of multiple cell lines expressing PAC features provide an important new resource for biological and preclinical therapeutic studies.

MeSH Terms
Adenocarcinoma/pathology Adult Animals Carcinoma/classification,pathology Cell Line DNA Probes Dexamethasone/pharmacology Glycoproteins/analysis Humans Lung Neoplasms/pathology,ultrastructure Mice Mice, Nude Proteolipids/analysis,genetics Pulmonary Surfactant-Associated Protein A Pulmonary Surfactant-Associated Proteins Pulmonary Surfactants/analysis,genetics Respiratory System/cytology,pathology Transplantation, Heterologous Tumor Cells, Cultured/cytology,drug effects,metabolism
Chemicals
DNA Probes Glycoproteins Proteolipids Pulmonary Surfactant-Associated Protein A Pulmonary Surfactant-Associated Proteins Pulmonary Surfactants Dexamethasone
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Gazdar A F
NCI-Navy Medical Oncology Branch, National Cancer Institute and Naval Hospital, Bethesda, Maryland 20814.
Linnoila R I
Kurita Y
Oie H K
Mulshine J L
Clark J C
Whitsett J A
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
1990-09-01
Pages
5481-7
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]