Evidence map›Paper›PMID 41781864›Full record

ArticleBMC microbiology2026

Microbiota characteristics in different lung tissue sites of female patients with invasive adenocarcinoma.

Da-Qian Sun, Cheng-Cheng Du, Jing-Shuo Li, Yu-Xian Chen, Hong Meng, Chun-Hai Li, Fan-Lei Kong

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Da-Qian Sun *Department of Radiology, Qilu Hospital of Shandong University, Jinan, 250012, China.
Cheng-Cheng Du *Department of Radiology, Qilu Hospital of Shandong University, Jinan, 250012, China.ORCID 0009-0008-8273-4847
Jing-Shuo LiDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, 250012, China.
Yu-Xian ChenCheeloo College of Medicine, Shandong University, Jinan, China.ORCID 0009-0001-2125-1410
Hong MengDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, 250012, China.ORCID 0009-0007-9390-8550
Chun-Hai LiDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, 250012, China.ORCID 0009-0009-7699-4973
Fan-Lei KongDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, 250012, China. kongfanlei_md@126.com.ORCID 0000-0003-2501-4620

Funding

Natural Science Foundation of Shandong Province ZR2023QH328
6 · The paper itself

Abstract

backgroundThis study aimed to analyze and compare the differences of microbiota in different parts of lung in women with invasive lung adenocarcinoma and further clarify the characteristics of microbiota changes in tumor microenvironment (TME).

methodsThe study patients were all female who underwent lung surgery in our hospital between October 2021 and October 2022. The feasibility of tissue sampling was evaluated by imaging before surgery. Cancerous tissue, paracancerous tissue and normal lung tissue samples were collected from female patients pathologically diagnosed with invasive adenocarcinoma. 16SrRNA sequencing technology was used to detect the diversity, composition distribution and functional characteristics of microbiota in tissue samples.

resultsThere was no significant difference in alpha diversity among bacterial communities at different lung locations in patients with invasive adenocarcinoma (p > 0.05), although a decreasing trend was observed in the Chao1 and ACE indices. Beta diversity analysis revealed that the microbial communities in cancerous and adjacent non-cancerous tissues exhibited similar structures (UniFrac PCoA: p > 0.05), but differed in species abundance (Unweighted UniFrac PCoA: p < 0.05). The microbiota composition is similar across different sites of invasive adenocarcinoma, but differs in species abundance. Compared to normal lung tissue, both tumor and paracancerous tissues show reduced overall species abundance, though Acinetobacter and Comamonas are significantly enriched (p<0.05). Functional predictions further indicated a shift in the tumor microenvironment, with an increase in Gram-negative bacteria, a decrease in Gram-positive bacteria, and a reduction in most microbial metabolic pathways.

conclusionsIn different locations in the lungs of patients with invasive adenocarcinoma, the compositional structure and functional characteristics of the microbiota of cancer and paracancerous tissues were similar and differed significantly from those of normal lung tissues. Species abundance was significantly lower in cancer and paracancerous tissues, with a dominance of Gram-negative bacteria and a reduced abundance of metabolic pathways in the microbiota.

Indexed as

Adenocarcinoma of LungBacteriaLungLung NeoplasmsMicrobiotaAdultAgedDNA, BacterialFemaleHumansMiddle AgedRNA, Ribosomal, 16STumor MicroenvironmentDNA, BacterialRNA, Ribosomal, 16S16SrRNAGram-negative bacteriaInvasive lung adenocarcinomaMicrobiota

Identifiers

PMID41781864
PMCPMC13069727

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.