Subtype-Based Microbial Analysis in Non-small Cell Lung Cancer

Hye Jin Jang; Eunkyung Lee; Young-Jae Cho; Sang Hoon Lee

doi:10.4046/trd.2022.0149

Tuberc Respir Dis > Volume 86(4); 2023 > Article

Jang, Lee, Cho, and Lee: Subtype-Based Microbial Analysis in Non-small Cell Lung Cancer

Original Article

Lung Cancer

Tuberculosis and Respiratory Diseases 2023;86(4):294-303.

Published online: June 22, 2023

DOI: https://doi.org/10.4046/trd.2022.0149

Subtype-Based Microbial Analysis in Non-small Cell Lung Cancer

Hye Jin Jang, MD.^1,²

, Eunkyung Lee, M.S.³, Young-Jae Cho, M.D., M.P.H., Ph.D.⁴, Sang Hoon Lee, M.D., Ph.D.¹

¹Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea

²Department of internal medicine, Myongji Hospital, Hanyang University College of Medicine, Goyang-si, Gyeonggi-do, Republic of Korea

³Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju, Republic of Korea

⁴Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea

Address for correspondence Sang Hoon Lee, M.D., Ph.D. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Institute of Chest Diseases, Severance Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea Phone 82-2-2228-1955 Fax 82-2-393-6884 E-mail cloud9@yuhs.ac

Received November 18, 2022 Revised April 17, 2023 Accepted June 18, 2023

It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/).

Abstract

Background

The human lung serves as a niche for a unique and dynamic bacterial community related to the development and aggravation of multiple respiratory diseases. Therefore, identifying the microbiome status is crucial to maintaining the microecological balance and maximizing the therapeutic effect on lung diseases. Therefore, we investigated the histological type-based differences in the lung microbiomes of patients with lung cancer.

Methods

We performed 16S rRNA sequencing to evaluate the respiratory tract microbiome present in bronchoalveolar lavage fluid. Patients with non-small cell lung cancer were stratified based on two main subtypes of lung cancer: adenocarcinoma and squamous cell carcinoma (SqCC).

Results

Among the 84 patients analyzed, 64 (76.2%) had adenocarcinoma, and 20 (23.8%) had SqCC. The α- and β-diversities showed significant differences between the two groups (p=0.004 for Chao1, p=0.001 for Simpson index, and p=0.011 for PERMANOVA). Actinomyces graevenitzii was dominant in the SqCC group (linear discriminant analysis [LDA] score, 2.46); the populations of Haemophilus parainfluenza (LDA score, 4.08), Neisseria subflava (LDA score, 4.07), Porphyromonas endodontalis (LDA score, 3.88), and Fusobacterium nucleatum (LDA score, 3.72) were significantly higher in the adenocarcinoma group.

Conclusion

Microbiome diversity is crucial for maintaining homeostasis in the lung environment, and dysbiosis may be related to the development and prognosis of lung cancer. The mortality rate was high, and the microbiome was not diverse in SqCC. Further large-scale studies are required to investigate the role of the microbiome in the development of different lung cancer types.

Keywords: Microbiome; Non-small Cell Lung Cancer; Diversity

Introduction

The human body, including the gut, skin, and other mucosal environments, is colonized by several microorganisms [1], and the interaction between these microbiomes and the immune system has been continuously studied. In healthy individuals, this interaction can contribute to immune homeostasis and susceptibility to infectious and inflammatory diseases [2].

The human lung serves as a niche for a unique and dynamic bacterial community related to the development of multiple respiratory diseases, such as chronic obstructive pulmonary disease [3], tuberculosis [4], idiopathic pulmonary fibrosis, and cystic fibrosis [5]. The lung microbiota is essential for barrier function, immune homeostasis, and anticancer immune surveillance via tumor antigenicity in healthy individuals [6]. Bacteria may disrupt the cell cycle by toxin production, resulting in cell growth with alterations in protein expression controlling DNA repair, cell division, and apoptosis [7], thus influencing the host immune response against malignant cells and promoting disease and cancer development [8]. These include Papillomaviridae, causing cervical cancer; Helicobacter pylori, contributing to non-cardia gastric cancer; and Schistosoma hematobium, responsible for bladder cancer [6].

Lung cancer is one of the most common cancers worldwide and is a leading cause of cancer-related morbidity [9]. Lung cancer is a complicated disease caused by interactions between host and environmental factors [10]. Among these risk factors, the microbiome plays a vital role in maintaining microecological balance and regulating host immune responses [11]. Recent studies using next-generation sequencing have revealed that the lung microbiome in patients with lung cancer differs from that in healthy individuals and that these microbiomes play a crucial role in immunity as well as cancer [12]. Therefore, understanding the mechanisms by which microbes present in the airways can influence lung cancer development and treatment could be beneficial to predicting cancer risk and improving treatment efficacy and safety [8].

Non-small cell lung carcinoma (NSCLC) is mainly classified into squamous cell carcinoma (SqCC), adenocarcinoma, and large cell carcinoma. The most common type of lung cancer is adenocarcinoma, which comprises approximately 40% to 60% of all lung cancer cases, whereas SqCC comprises 25% to 30% of all lung cancer cases [13]. Large cell (undifferentiated) carcinomas account for 5% to 10% of lung cancers and are relatively rare. Several genetic alterations, including activating mutations in epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), c-ros oncogene 1 (ROS1), rat sarcoma (RAS), and v-raf murine sarcoma viral oncogene homolog B1 (BRAF), have been identified as drivers of tumorigenesis in NSCLC [14]. Although overall survival has improved owing to the use of targeted therapy for NSCLC patients with driver mutations and the introduction of immunotherapy, resistance eventually develops after using targeted anticancer agents for a certain period; additionally, targeted therapy for SqCC is limited [15]. Furthermore, only a small portion of patients with lung cancer achieve optimal and sustained efficacy from immunotherapy. There is no effective anticancer drug for patients who are resistant to immunotherapy, and the prognosis is poor [16]. Therefore, identifying the microbiome status is crucial to maintaining the microecological balance within the lungs, which could prevent the progression of lung cancer and maximize the effect of immunotherapy in NSCLC.

In this study, we aimed to investigate the microbial differences in patients with NSCLC according to the different subtypes of SqCC and adenocarcinoma, which are predominant in NSCLC.

Materials and Methods

1. Patient recruitment and sample collection

A total of 84 patients who were pathologically diagnosed with NSCLC were recruited from June 1, 2018, to June 31, 2020. Patients admitted for a lung cancer diagnosis in two tertiary hospitals—the Severance Hospital and Seoul National University Bundang Hospital, in South Korea. A bronchoscopy specialist collected bronchoalveolar lavage (BAL) fluid samples using a sterile bronchoscope.

2. Sample collection

Before bronchoscopy, all patients washed their mouths twice with a sterile saline solution. The patients were given topical anesthesia (lidocaine) using a nebulizer. Subsequently, patients were administered with midazolam and fentanyl, as recommended [17]. The bronchoscope was placed into the mouth of the patients and then placed into the lungs. BAL fluid was obtained according to a standardized protocol: when the bronchoscope arrived in the “involved” airway containing lung masses or lung nodules, the bronchi were flushed with 30 to 50 mL of sterile saline (0.9%). Approximately 15 mL of BAL fluid samples were obtained from each patient for sequencing analysis. BAL fluid samples were immediately placed at -70°C in a freezer, and DNA extraction was conducted within 24 hours.

3. DNA extraction, polymerase chain reaction amplification, and sequencing

According to the manufacturer’s instructions, total DNA was extracted using the Maxwell RSC PureFood GMO and Authentication Kit (Promega, Madison, WI, USA). We performed polymerase chain reaction (PCR) amplification using fusion primers which were targeting the V3-V4 regions of the 16S rRNA gene of the extracted DNA. The fusion primers 341F (5’-AATGATACGGCG ACCACCGAGATCTACAC-XXXXXXXXTCGTCGGCAGCG TC-AGATGTGTATAAGAGACAG-CCTACGGGNGGCWG CAG-3’) and 805R (5’-CAAGCAGAAGACGGCATACGA GAT-XXXXXXXXGTCTCGTGGGCTCGG-AGATGTGTATA AGAGACAG-GACTACHVGGGTATCTAATCC-3’) were used for bacterial amplification; the underlined sequence indicates the target region of the primer. We performed amplification under the following conditions: initial denaturation at 95°C for 3 minutes followed by 25 cycles of denaturation at 95°C for 30 seconds, primer annealing at 55°C for 30 seconds, extension at 72°C for 30 seconds, and a final elongation step at 72°C for 5 minutes.

The PCR product was identified by performing 1% agarose gel electrophoresis and visualized using the Gel Doc system (BioRad, Hercules, CA, USA). The amplified products were purified using a CleanPCR kit (CleanNA, Waddinxveen, Netherlands). The purified products at the same concentrations were pooled, and short fragments (non-target products) were cleared using CleanPCR. We assessed quality and product size with a Bioanalyzer 2100 (Agilent Technologies, Palo Alto, CA, USA) using a DNA 7500 chip. Following the manufacturer’s instructions, mixed amplicons were pooled, and sequencing was performed at CJ Bioscience, Inc. (Seoul, Korea) using an Illumina MiSeq Sequencing system (Illumina, San Diego, CA, USA). Detailed methods are described in the Supplementary Materials and Methods.

4. Statistical analysis

Categorical variables are reported as numbers (percentages). Continuous variables with normal distribution are reported as mean±standard deviation, while variables with abnormal distribution are reported as median with interquartile ranges (25th-75th percentiles). Depending on the normality of distribution, categorical variables were compared using the chi-square test, and continuous variables were compared using either an independent t-test or Mann-Whitney U test. p-values <0.05 were considered statistically significant. All statistical analyses were performed with IBM SPSS Statistics version 25.0 (IBM, Armonk, NY, USA).

5. Ethics approval and patient consent

The study protocol was approved by the Institutional Review Board of Severance Hospital, South Korea (IRB No. 4-0018-0313) and Seoul National University Bundang Hospital, South Korea (IRB No. B-1610/365-302). The study design was approved by the appropriate ethical review committee, and we obtained informed consents was from all participants.

Results

1. Patient characteristics

The patients were divided into two groups according to their pathologic subtype: adenocarcinoma and SqCC. The baseline characteristics of the two groups are listed in Table 1. The adenocarcinoma group had 64 patients (76.2%), and 20 (23.8%) belonged to the SqCC group. The mean age was 66.7±11.2 years, and the patients in the SqCC group were older (p=0.033). Male gender (51.6% vs. 95.0%) and smoking history (46.9% vs. 90.0%) were dominant in the SqCC group, and the mortality rate was significantly higher in the SqCC group (6.3% vs. 25%, p=0.035).

2. Taxonomy composition in patients with lung cancer based on pathological subtypes

Figure 1 depict the differences between lung microbiomes according to the pathological type. The dominant phyla in the adenocarcinoma group were Bacteroidetes (40.8%), Proteobacteria (24.9%), Firmicutes (24.1%), Fusobacteria (6.0%), and Actinobacteria (2.8%). In the SqCC group, Bacteroidetes (35.0%), Firmicutes (29.3%), Proteobacteria (27.8%), Fusobacteria (3.8%), and Actinobacteria (3.3%) were dominant.

The abundance of Fusobacteria differed between the adenocarcinoma and SqCC groups (Wilcoxon test, p=0.024) (Figure 2A), whereas that of Firmicutes, Bacteroidetes, and Proteobacteria were not statistically significant (Figure 2B-D). The abundance-based coverage estimator, Shannon, and Simpson indices were evaluated to estimate α-diversity in the lung microbiome, which summarizes the structure of an ecological community with respect to its richness (number of taxonomic groups), evenness (distribution of abundances of the groups), or both [18]. The operational taxonomic units of both groups exhibited statistically significant differences (p=0.006) (Figure 3A). Species richness differed between the two groups based on Chao1 (p=0.004) (Figure 3B), Simpson (p=0.001) (Figure 3C), and Shannon indices (p=0.0002) (Figure 3D).

Principal coordinate analysis (PCoA) was performed to examine the similarity between the bacterial communities in each group. The Bray-Curtis distance was calculated to estimate the β-diversity in the lung taxonomy community structure in patients with NSCLC, which provides a measure of the degree to which samples differ from one another and can help elucidate the aspects of microbial ecology that are not apparent from the composition of individual samples [19]. A significant difference according to the pathological type was observed between the groups (p=0.011) (Figure 4).

We performed linear discriminant analysis (LDA) effect size (LEfSe) analysis to further evaluate the differences in these dominant genera between patients with NSCLC in the adenocarcinoma and SqCC groups, suggesting that the genus Actinomyces, which belongs to the phylum Actinobacteria, was significantly more abundant in the SqCC group (Wilcoxon test, p=0.049) (Figure 5). The genus with the greatest influence on the distinction between the two groups, with LDA score of 4.08, was Haemophilus, belonging to the Proteobacteria phylum (Figure 5).

Neisseria subflava, belonging to Proteobacteria, was dominant in the adenocarcinoma group with an LDA score of 4.07 (Wilcoxon test, p=0.029). These were followed by Porphyromonas and Fusobacterium with LDA scores of 3.88 (p<0.001) and 3.72 (p<0.001), respectively, in the adenocarcinoma group (Figure 5).

Discussion

In this study, we characterized lung cancer microbiota by analyzing BAL in patients with NSCLC from two hospitals using 16S rRNA sequencing. The diversity of microbiome was significantly reduced in SqCC comparing with adenocarcinoma.

Recent research has suggested strong associations between lung cancer and specific microorganisms through different mechanisms, including induction of host inflammatory pathways, production of bacterial toxins that alter host genomic stability, and release of cancer-promoting microbial metabolites [20]. For example, Veillonella is present in patients with lung cancer and plays a role in NSCLC pathogenesis [21]. It also plays a role in the increased infiltration of inflammatory cells (Th17 cells) and upregulation of the extracellular signal-regulated kinase/phosphoinositide 3-kinase (ERK/PI3K) pathway in bronchial epithelial cells [22]. Notably, PI3K pathway upregulation was previously shown to be an early pathogenic event in NSCLC, regulating cell proliferation, survival, differentiation, and invasion [23]. Concordantly, our study further revealed significant differences in the microbiome in NSCLC according to different pathologic types (adenocarcinoma and SqCC) exhibiting different prognoses.

Fusobacteria was a significantly abundant phylum in the adenocarcinoma group, and Proteobacteria was abundant in both groups; however, the abundance of certain species was different. Haemophilus parainfluenza, belonging to Proteobacteria, was the most dominant species in the adenocarcinoma group and is known to cause various invasive, chronic, and recurrent diseases [24]. A previous study revealed that the abundance of H. parainfluenza significantly differed between healthy individuals and patients with lung cancer [25]. We further found that it was more abundant in the adenocarcinoma group than in the SqCC group.

Porphyromonas endodontalis, belonging to Bacteroidetes, is known to be elevated in the sputum of patients with early lung cancer [26]. In our study, the proportion of early lung cancer (stage I/II) was higher in patients with adenocarcinoma (51.6% vs. 20.0%). Porphyromonas gingivalis, which belongs to the same phylum as P. endodontalis, promotes the survival and proliferation of epithelial cells by increasing PI3K/Akt signaling shortly after an infection, resulting in the inhibition of intrinsic apoptosis and increased expression of cancer stem cell markers CD44 and CD133 [27]. Although P. endodontalis has not yet been well studied, our study revealed its enhanced abundance in patients with adenocarcinoma, similar to P. gingivalis in oral cancer.

Neisseria species are associated with infections such as septic arthritis [28] and meningitis [29] among them, N. subflava is increased in patients with oral cavity cancer [30]. Fusobacterium nucleatum was also increased in oral cancers [31]. It promotes oral cavity cancer via direct interaction with oral epithelial cells through Toll-like receptors, increasing the expression of Toll-like receptor 2 (TLR2) in oral squamous cell carcinoma (OSCC) cells and interleukin 6 (IL-6) in cells and a mouse model [32]. F. nucleatum in esophageal cancer tissues has been associated with shorter survival, suggesting its potential role as a prognostic biomarker, which might also contribute to aggressive tumor behavior by activating chemokines, such as chemokine (C-C motif) ligand 20 [33]. The oral microbiome is correlated with the lung microbiome because the lungs are directly connected to the oral cavity [34]; thus, we can infer that N. subflava and F. nucleatum are associated with the development of lung cancer, especially adenocarcinoma. The microbiome was diverse in the adenocarcinoma group and similar to the microbiota of oral cavity cancer, suggesting that the oral microbial environment plays a crucial role in patients with genetic susceptibility to lung cancer development.

SqCC is associated with male smokers [35] and certain pathogens, such as that causing tuberculosis [36]. In patients with SqCC, Actinomyces graevenitzii was much more abundant than in the adenocarcinoma group. A. graevenitzii is a component of the oropharyngeal flora and is associated with pulmonary infections in some cases [37]; however, it has not yet been comprehensively studied. Our study revealed that it is related to SqCC.

Previous studies have reported differences in the clinical characteristics and treatment methods between the two subtypes [38]. Wang et al. [39] analyzed clinical characteristics of 48,296 patients with lung cancer by dividing them into adenocarcinoma and SqCC groups. The two groups differed significantly in many clinical characteristics, including age, sex, clinical/pathological stage, and treatment. Notably, they reported that the stage-specific 5-year overall survival rate differed significantly between the two groups even after propensity score matching, suggesting that the two cancers should be analyzed separately to provide a precise outcome. Similarly, our study identified significantly different microbiomes and PCoA plots depending on the cancer subtype. Furthermore, the microbiome was significantly more diverse in the adenocarcinoma group than that in the SqCC group. Also, there was significant difference of α-diversity between early (stage 1, 2 and 3a) and late stage (stage 3b and 4) of NSCLC (Supplementary Figure S1). As the microbiome plays a vital role in barrier function and immune surveillance, this low microbial diversity may also be related to the poor prognosis of SqCC.

Although diet and antibiotics usage, which might influence the microbial composition, were not investigated, a specialized bronchoscopist conducted sterile bronchoscopy, and we used 16S rRNA sequencing during the first diagnosis, which was prospective, informative, and sensitive compared with other conventional methods.

In conclusion, we identified that the microbial α- and β-diversities were different between the two types of lung cancer. H. parainfluenzae, N. subflava, P. endodontalis, and F. nucleatum were significantly abundant in the adenocarcinoma group, whereas A. graevenitzii was abundant in the SqCC group. Prolonged colonization and subsequent inflammation may disrupt the normal host immune barrier, eventually leading to cancer development. Further large-scale studies are required to determine the role of the microbiome in the development of different lung cancer types.

Notes

Authors’ Contributions

Conceptualization: Jang HJ, Cho YJ, Lee SH. Methodology: Jang HJ, Lee EK, Cho YJ, Lee SH. Formal analysis: Jang HJ, Lee EK, Cho YJ, Lee SH. Data curation: Jang HJ, Lee SH. Software: Lee SH. Validation: Jang HJ, Cho YJ, Lee SH. Investigation: Lee SH. Writing - original draft preparation: Jang HJ, Cho YJ, Lee SH. Writing - review and editing: Jang HJ, Lee EK, Cho YJ, Lee SH. Approval of final manuscript: all authors.

Conflicts of Interest

No potential conflict of interest relevant to this article was reported.

Funding

This Study was Supported by a 2021-Grant from The Korean Academy of Tuberculosis and Respiratory Diseases.

Supplementary Material

Supplementary material can be found in the journal homepage (http://www.e-trd.org).

Supplementary Materials and Methods

trd-2022-0149-Supplementary-Materials-and-Methods.pdf

Supplementary Figure S1.

Comparison of the α-diversity in bronchoalveolar lavage (BAL) fluid microbiomes between early and late stage of non-small cell lung carcinoma.

trd-2022-0149-Supplementary-Fig-1.pdf

Figure 1.

Taxonomic composition of the microbiome community between subgroups. (A) Dominant phyla based on the types of non-small cell lung carcinoma (NSCLC). (B) Dominant genera based on the types of NSCLC. SqCC: squamous cell carcinoma; ETC: et cetera.

Figure 2.

Differential abundances of phyla. (A) Fusobacteria, (B) Firmicutes, (C) Bacteroidetes, and (D) Proteobacteria between the adenocarcinoma and squamous cell carcinoma (SqCC) groups.

Figure 3.

Comparison of the α-diversity in bronchoalveolar lavage (BAL) fluid microbiomes between the adenocarcinoma and squamous cell carcinoma (SqCC) groups. (A) Number of operational taxonomic units (OTUs), (B) Chao1 index, (C) Simpson index, and (D) Shannon index. Upper box, 2nd quartile; midline, median; lower box, 3rd quartile; whiskers, highest and lowest quartiles.

Figure 4.

Principal coordinate analysis (PCoA) plot based on the Bray-Curtis (BC) distance of the BAL fluid microbiome between the adenocarcinoma and squamous cell carcinoma (SqCC) groups. PC: principal component.

Figure 5.

Linear discriminant analysis (LDA) effect size (LEfSe) analysis of the dominant genera between adenocarcinoma and squamous cell carcinoma (SqCC) groups. The blue and red bars indicate the taxa identified in greater relative abundance in patients with adenocarcinoma and SqCC, respectively.

Table 1.

Demographics and clinical characteristics of patients

Characteristic	Adenocarcinoma	SqCC	Total	p-value
Number	64 (76.2)	20 (23.8)	84 (100.0)
Age, yr	65.2±10.5	71.5±11.1	66.7±11.2	0.033
Gender				<0.001
Male	33 (51.6)	19 (95.0)	52 (61.9)
Female	31 (48.4)	1 (5.0)	32 (38.1)
Smoking history				0.001
Current or former	30 (46.9)	18 (90.0)	48 (57.1)
Never	34 (53.1)	2 (10.0)	36 (42.9)
Smoking amount, pack-yr	28.2±15.0	37.0±14.9	31.5±15.4	0.055
Neutrophil-lymphocyte ratio	4.76 (1.83-6.27)	2.87 (1.95-5.31)	3.05 (1.91-5.85)	0.423
Stage
I/II/III/IV	25/8/14/17	2/2/9/7	27/10/23/24
Mortality	4 (6.3)	5 (25.0)	9 (10.7)	0.035

Values are presented as number (%), mean±standard deviation, or median (interquartile range).

SqCC: squamous cell carcinoma.

References

1. Sender R, Fuchs S, Milo R. Are we really vastly outnumbered?: revisiting the ratio of bacterial to host cells in humans. Cell 2016;164:337-40.

2. Zheng D, Liwinski T, Elinav E. Interaction between microbiota and immunity in health and disease. Cell Res 2020;30:492-506.

3. Jubinville E, Veillette M, Milot J, Maltais F, Comeau AM, Levesque RC, et al. Exacerbation induces a microbiota shift in sputa of COPD patients. PLoS One 2018;13:e0194355.

4. Naidoo CC, Nyawo GR, Wu BG, Walzl G, Warren RM, Segal LN, et al. The microbiome and tuberculosis: state of the art, potential applications, and defining the clinical research agenda. Lancet Respir Med 2019;7:892-906.

5. Kitsios GD, Rojas M, Kass DJ, Fitch A, Sembrat JC, Qin S, et al. Microbiome in lung explants of idiopathic pulmonary fibrosis: a case-control study in patients with endstage fibrosis. Thorax 2018;73:481-4.

6. Zitvogel L, Ayyoub M, Routy B, Kroemer G. Microbiome and anticancer immunosurveillance. Cell 2016;165:276-87.

7. Apopa PL, Alley L, Penney RB, Arnaoutakis K, Steliga MA, Jeffus S, et al. PARP1 is up-regulated in non-small cell lung cancer tissues in the presence of the cyanobacterial toxin microcystin. Front Microbiol 2018;9:1757.

8. Ramirez-Labrada AG, Isla D, Artal A, Arias M, Rezusta A, Pardo J, et al. The influence of lung microbiota on lung carcinogenesis, immunity, and immunotherapy. Trends Cancer 2020;6:86-97.

9. Islami F, Torre LA, Jemal A. Global trends of lung cancer mortality and smoking prevalence. Transl Lung Cancer Res 2015;4:327-38.

10. Brandi G, Frega G. Microbiota: overview and implication in immunotherapy-based cancer treatments. Int J Mol Sci 2019;20:2699.

11. Liu NN, Ma Q, Ge Y, Yi CX, Wei LQ, Tan JC, et al. Microbiome dysbiosis in lung cancer: from composition to therapy. NPJ Precis Oncol 2020;4:33.

12. Cameron SJ, Lewis KE, Huws SA, Hegarty MJ, Lewis PD, Pachebat JA, et al. A pilot study using metagenomic sequencing of the sputum microbiome suggests potential bacterial biomarkers for lung cancer. PLoS One 2017;12:e0177062.

13. Zappa C, Mousa SA. Non-small cell lung cancer: current treatment and future advances. Transl Lung Cancer Res 2016;5:288-300.

14. Shroff GS, de Groot PM, Papadimitrakopoulou VA, Truong MT, Carter BW. Targeted therapy and immunotherapy in the treatment of non-small cell lung cancer. Radiol Clin North Am 2018;56:485-95.

15. Mamdani H, Matosevic S, Khalid AB, Durm G, Jalal SI. Immunotherapy in lung cancer: current landscape and future directions. Front Immunol 2022;13:823618.

16. Blach J, Wojas-Krawczyk K, Nicos M, Krawczyk P. Failure of immunotherapy: the molecular and immunological origin of immunotherapy resistance in lung cancer. Int J Mol Sci 2021;22:9030.

17. Du Rand IA, Blaikley J, Booton R, Chaudhuri N, Gupta V, Khalid S, et al. British Thoracic Society guideline for diagnostic flexible bronchoscopy in adults: accredited by NICE. Thorax 2013;68 Suppl 1:i1-44.

18. Willis AD. Rarefaction, alpha diversity, and statistics. Front Microbiol 2019;10:2407.

19. Goodrich JK, Di Rienzi SC, Poole AC, Koren O, Walters WA, Caporaso JG, et al. Conducting a microbiome study. Cell 2014;158:250-62.

20. Kovaleva OV, Romashin D, Zborovskaya IB, Davydov MM, Shogenov MS, Gratchev A. Human lung microbiome on the way to cancer. J Immunol Res 2019;2019:1394191.

21. Chen J, Domingue JC, Sears CL. Microbiota dysbiosis in select human cancers: evidence of association and causality. Semin Immunol 2017;32:25-34.

22. Segal LN, Clemente JC, Tsay JC, Koralov SB, Keller BC, Wu BG, et al. Enrichment of the lung microbiome with oral taxa is associated with lung inflammation of a Th17 phenotype. Nat Microbiol 2016;1:16031.

23. Gustafson AM, Soldi R, Anderlind C, Scholand MB, Qian J, Zhang X, et al. Airway PI3K pathway activation is an early and reversible event in lung cancer development. Sci Transl Med 2010;2:26ra25.

24. Tufvesson E, Bjermer L, Ekberg M. Patients with chronic obstructive pulmonary disease and chronically colonized with Haemophilus influenzae during stable disease phase have increased airway inflammation. Int J Chron Obstruct Pulmon Dis 2015;10:881-9.

25. Kosikowska U, Biernasiuk A, Rybojad P, Los R, Malm A. Haemophilus parainfluenzae as a marker of the upper respiratory tract microbiota changes under the influence of preoperative prophylaxis with or without postoperative treatment in patients with lung cancer. BMC Microbiol 2016;16:62.

26. Druzhinin VG, Matskova LV, Demenkov PS, Baranova ED, Volobaev VP, Minina VI, et al. Taxonomic diversity of sputum microbiome in lung cancer patients and its relationship with chromosomal aberrations in blood lymphocytes. Sci Rep 2020;10:9681.

27. Olsen I, Yilmaz O. Possible role of Porphyromonas gingivalis in orodigestive cancers. J Oral Microbiol 2019;11:1563410.

28. Schaad UB. Arthritis in disease due to Neisseria meningitidis. Rev Infect Dis 1980;2:880-8.

29. Durand ML, Calderwood SB, Weber DJ, Miller SI, Southwick FS, Caviness VS Jr, et al. Acute bacterial meningitis in adults: a review of 493 episodes. N Engl J Med 1993;328:21-8.

30. Al-Hebshi NN, Nasher AT, Idris AM, Chen T. Robust species taxonomy assignment algorithm for 16S rRNA NGS reads: application to oral carcinoma samples. J Oral Microbiol 2015;7:28934.

31. Su SC, Chang LC, Huang HD, Peng CY, Chuang CY, Chen YT, et al. Oral microbial dysbiosis and its performance in predicting oral cancer. Carcinogenesis 2021;42:127-35.

32. Binder Gallimidi A, Fischman S, Revach B, Bulvik R, Maliutina A, Rubinstein AM, et al. Periodontal pathogens Porphyromonas gingivalis and Fusobacterium nucleatum promote tumor progression in an oral-specific chemical carcinogenesis model. Oncotarget 2015;6:22613-23.

33. Yamamura K, Baba Y, Nakagawa S, Mima K, Miyake K, Nakamura K, et al. Human microbiome fusobacterium nucleatum in esophageal cancer tissue is associated with prognosis. Clin Cancer Res 2016;22:5574-81.

34. Xu N, Wang L, Li C, Ding C, Li C, Fan W, et al. Microbiota dysbiosis in lung cancer: evidence of association and potential mechanisms. Transl Lung Cancer Res 2020;9:1554-68.

35. Shiels MS, Albanes D, Virtamo J, Engels EA. Increased risk of lung cancer in men with tuberculosis in the alpha-tocopherol, beta-carotene cancer prevention study. Cancer Epidemiol Biomarkers Prev 2011;20:672-8.

36. Arulanantham A, Jayarajah U, Dharmasiri R, Jeyanthakumar R, Siriwardena KN, Ilangamge S. Squamous cell carcinoma in the post tuberculosis lung after 30 years of treatment completion. Case Rep Surg 2020;2020:8570212.

37. Gliga S, Devaux M, Gosset Woimant M, Mompoint D, Perronne C, Davido B. Actinomyces graevenitzii pulmonary abscess mimicking tuberculosis in a healthy young man. Can Respir J 2014;21:e75-7.

38. Ettinger DS, Wood DE, Aisner DL, Akerley W, Bauman JR, Bharat A, et al. Non-small cell lung cancer, version 3.2022, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw 2022;20:497-530.

39. Wang BY, Huang JY, Chen HC, Lin CH, Lin SH, Hung WH, et al. The comparison between adenocarcinoma and squamous cell carcinoma in lung cancer patients. J Cancer Res Clin Oncol 2020;146:43-52.

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Korean Academy of Tuberculosis and Respiratory Diseases

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