H-209
Cat.No.: CSC-C0510
Species: Homo sapiens (Human)
Source: Bone Marrow Metastasis
Morphology: spherical-to-ovoid cells growing singly in large clumps
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Immunology: cytokeratin +, cytokeratin-7 -, cytokeratin-8 +, cytokeratin-17 -, cytokeratin-18 +, cytokeratin-19 +, desmin -, endothel -, EpCAM +, GFAP -, neurofilament -, vimentin -
Viruses: PCR
The H209 cell line, also known as NCI-H209, is a classical human Small Cell Lung Cancer (SCLC) cell line developed by Gazdar and coworkers in 1979. It was obtained from the site of metastasis of a 55-year-old white male in the bone marrow before any treatment. The line is genetically hyperdiploid with a median chromosomal number of 49 and has homozygous mutations in RB1(p.Cys706Phe) and TP53(c.673-2A>T) gene.
In H209 cells display an unusual growth behavior in culture, growing as tight, spherical aggregates in suspension instead of attaching to the flask surface. Only cells within these aggregates remain alive, but the culture media generally contains a considerable quantity of cellular debris, a normal characteristic of this line. H209 is a neuroendocrine tumor model that expresses high levels of typical SCLC indicators such neuron-specific enolase, creatine kinase-BB, L-DOPA decarboxylase, and bombesin-like immunoreactivity.
It is normally cultured in a serum-supplemented rich basal media under conventional conditions (37°C, 5% CO2). The H209 line is widely used in oncology research for the study of SCLC pathology, neuroendocrine differentiation, drug screening and tumor biology due to its unique biological characteristics.
STAT3 and YAP Expression in Small Cell Lung Cancer Lines
Small cell lung cancer (SCLC) is an aggressive malignancy with poor prognosis, yet the interplay between key oncogenic pathways remains unclear. While STAT3 and YAP are established drivers of tumor progression, their potential interaction in SCLC pathogenesis is undefined.
Western blot analysis revealed that among four SCLC cell lines, H209 cells uniquely exhibited concurrent high expression of both phosphorylated STAT3 (p-STAT3) and YAP protein compared to H146, H446, and H720 cells (Figure 1A-C). This molecular profile correlated with distinct phenotypic behavior: H209 cells displayed an adherent growth pattern, whereas the other cell lines with low p-STAT3/YAP expression exhibited a characteristic floating growth pattern (Figure 1D). These data suggest a potential link between STAT3/YAP signaling and the adhesive phenotype in SCLC.

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