<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE169029" accession="SRP310923">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP310923</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA714926</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE169029</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>TGF-ß signaling activated by cancer-associated fibroblasts determines the histological signature of lung adenocarcinoma</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Invasive lung adenocarcinoma (LADC) is classified histologically as lepidic, acinar, papillary, micropapillary, or solid. We found that A549 human LADC cells formed tumors with distinct histological features—solid-type or acinar-type tumors—depending on the site of development in immunodeficient mice and that a solid-to-acinar transition (SAT) could be induced by cancer-associated fibroblasts (CAFs) in 3D cocultures with A549. To clarify the molecular mechanisms contributing to SAT induction, we performed RNA-seq analysis of four A549 tumor cell samples derived from solid- or acinar-type tumor tissue formed in vivo or from 3D tumor colonies formed in the presence or absence of CAFs in vitro. Overall design: RNA-seq analysis of A549 cells isolated from solid-type or acinar-type tumors in immunodeficient mice by laser microdissection and  A549 cells isolated from 3D cocultures in the presence or absence of CAFs by cell sorting.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE169029</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>34289987</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
