Evidence map›Paper›PMID 40820472›Full record

ArticleMicrobiologyOpen2025

Assessing Diversity Scaling in Lung Cancer Microbiome Across Individuals and Tissue Types.

Jiandong Mei, Yuting Qiao, Zhanshan Sam Ma

Abstract read
In one paragraph

Article in MicrobiologyOpen, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jiandong MeiDepartment of Thoracic Surgery, West China Hospital, Sichuan University, Chengdu, China.ORCID 0000-0003-0842-5540
Yuting QiaoComputational Biology and Medical Ecology Lab, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China.ORCID 0000-0002-5084-3706
Zhanshan Sam MaComputational Biology and Medical Ecology Lab, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China.

Funding

This work was supported by the National Natural Science Foundation of China (NSFC Grant# 72274192) and the Prosperous Yunnan Talent Support Program.
6 · The paper itself

Abstract

The intra-tumor microbiome can impact the tumor's behavior by influencing its growth, inflammatory reactions, evasion of the immune system, genomic instability, and drug resistance. Altering this microbiota to improve the response to cancer treatment could offer fresh perspectives on cancer therapy. The very first step in intervening in the microbiome is to gain a deep understanding of how microbial diversity varies spatially and temporally between tissues or among individuals. Such changes can be investigated with the so-termed diversity-area relationship (DAR) modeling (Ma. 2018. Ecology and Evolution, 8(20), 10023-10038). This included examining the DAR profiles, Pairwise Diversity Overlap (PDO) profiles, Maximum Accumulated Diversity (MAD) profiles, and the ratio of local to global accumulated diversity (LGD) profiles. This study applies the DAR approach to reanalyze five lung tissue microbiome datasets to shed light on how the microbial diversity changes across tissue types and across individual patients. We characterized the diversity scaling of human lung cancer microbiota from aspects such as microbial community diversity, variation rates of diversity, similarity, and microbial community proportions. The generated results indicate that there are no statistically significant differences in the DAR scaling parameters across different tissue types, suggesting that the diversity scaling of microbial communities in normal and tumor tissues across individuals seems to be invariant. The invariance is simply a reflection of the resilience of lung tissue microbiome against disturbance such as lung cancer, and thus further studies at the level of microbial species to better understand their relationship with cancer are critical.

Indexed as

BiodiversityLung NeoplasmsMicrobiotaBacteriaHumansLungdiversity–area relationship (DAR)diversity scalinghuman lung cancer microbiomelung adenocarcinoma (LUAD)lung cancerlung squamous cell carcinoma (LUSC)

Identifiers

PMID40820472
PMCPMC12358694

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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.