Scholarlink

Background <p>Colorectal cancer (CRC) remains a major global health burden, ranking as the third most prevalent malignancy and the second leading cause of cancer-related mortality. Its pathogenesis involves complex interactions between genetic, environmental, and lifestyle factors, with emerging evidence implicating the gut microbiome as a key contributor. Specific pathobionts, such as <i>Escherichia coli</i> and Klebsiella pneumoniae, have been linked to CRC progression due to their pro-inflammatory properties. This study investigated the association of <i>E. coli</i> and <i>K. pneumoniae</i> with CRC tissues and their influence on oncogenic gene expression, particularly within the TGF-β, Notch, Wnt/β-catenin, Rho GTPase, and EGFR/MAPK signaling pathways.</p> Methods <p>Using both culture and molecular-based methods, we analyzed 100 CRC patient biopsies from Taleghani Hospital, Tehran (July 2021–May 2023), assessing bacterial presence and the expression of 19 CRC-associated genes. Adhesion and invasion capabilities of isolates were evaluated in Caco-2 cells.</p> Results <p>While clinical parameters (e.g., age, survival, tumor stage) did not differ significantly between bacterial groups, gene expression analysis revealed elevated <i>FOLH1</i> and <i>MAP2K1</i> in adhesive-invasive <i>K. pneumoniae</i> isolates and increased <i>FOLH1</i> in <i>E. coli</i>-positive samples. Tumor stage- and site-specific variations were observed, such as heightened <i>ANXA3</i> expression in Stage I tumors harboring <i>K. pneumoniae</i>. Principal component analysis (PCA) demonstrated overlapping oncogenic profiles, suggesting complex, context-dependent microbial influences.</p> Conclusions <p>Our findings indicate that <i>E. coli</i> and <i>K. pneumoniae</i> may exert nuanced, tumor-specific effects on oncogenic pathways, potentially mediated more by chronic inflammation than direct gene dysregulation. Further studies employing single-cell RNA sequencing are warranted to elucidate these interactions and their translational potential for CRC diagnostics and therapeutics.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Assessing the role of Escherichia coli and Klebsiella pneumoniae in colorectal cancer oncogene expression: insights from microbial colonization phenotypes

  • 期刊论文

  • 发表日期：

    2025年8月15日

查看全文
  • Samin Davoody,
  • Zahra Tayebi,
  • Mohsen Sharif-zak,
  • Mehdi Azizmohammad Looha,
  • Nazanin Mortezaei Ferizhandy,
  • Sahar Sadeghi Mofrad,
  • Hamidreza Houri

摘要

Background

Colorectal cancer (CRC) remains a major global health burden, ranking as the third most prevalent malignancy and the second leading cause of cancer-related mortality. Its pathogenesis involves complex interactions between genetic, environmental, and lifestyle factors, with emerging evidence implicating the gut microbiome as a key contributor. Specific pathobionts, such as Escherichia coli and Klebsiella pneumoniae, have been linked to CRC progression due to their pro-inflammatory properties. This study investigated the association of E. coli and K. pneumoniae with CRC tissues and their influence on oncogenic gene expression, particularly within the TGF-β, Notch, Wnt/β-catenin, Rho GTPase, and EGFR/MAPK signaling pathways.

Methods

Using both culture and molecular-based methods, we analyzed 100 CRC patient biopsies from Taleghani Hospital, Tehran (July 2021–May 2023), assessing bacterial presence and the expression of 19 CRC-associated genes. Adhesion and invasion capabilities of isolates were evaluated in Caco-2 cells.

Results

While clinical parameters (e.g., age, survival, tumor stage) did not differ significantly between bacterial groups, gene expression analysis revealed elevated FOLH1 and MAP2K1 in adhesive-invasive K. pneumoniae isolates and increased FOLH1 in E. coli-positive samples. Tumor stage- and site-specific variations were observed, such as heightened ANXA3 expression in Stage I tumors harboring K. pneumoniae. Principal component analysis (PCA) demonstrated overlapping oncogenic profiles, suggesting complex, context-dependent microbial influences.

Conclusions

Our findings indicate that E. coli and K. pneumoniae may exert nuanced, tumor-specific effects on oncogenic pathways, potentially mediated more by chronic inflammation than direct gene dysregulation. Further studies employing single-cell RNA sequencing are warranted to elucidate these interactions and their translational potential for CRC diagnostics and therapeutics.