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The associated risk of Blastocystis infection in cancer: A case control study

BACKGROUND: Blastocystis is an anaerobic intestinal protozoan. Nine Blastocystis subtypes (STs) were detected in humans. A subtype-dependent association between Blastocystis and different cancer types has been debated in many studies. Thus, this study aims to assess the possible association between...

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Autores principales: Labania, Lena, Zoughbor, Sumaya, Ajab, Suad, Olanda, Marie, Shantour, Sulaiman N. M., Al Rasbi, Zakeya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986623/
https://www.ncbi.nlm.nih.gov/pubmed/36890816
http://dx.doi.org/10.3389/fonc.2023.1115835
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author Labania, Lena
Zoughbor, Sumaya
Ajab, Suad
Olanda, Marie
Shantour, Sulaiman N. M.
Al Rasbi, Zakeya
author_facet Labania, Lena
Zoughbor, Sumaya
Ajab, Suad
Olanda, Marie
Shantour, Sulaiman N. M.
Al Rasbi, Zakeya
author_sort Labania, Lena
collection PubMed
description BACKGROUND: Blastocystis is an anaerobic intestinal protozoan. Nine Blastocystis subtypes (STs) were detected in humans. A subtype-dependent association between Blastocystis and different cancer types has been debated in many studies. Thus, this study aims to assess the possible association between Blastocystis infection and cancer, especially colorectal cancer (CRC). We also screened the presence of gut fungi and their association with Blastocystis. METHODS: We used a case-control design; cancer patients and cancer-free (CF) participants. The cancer group was further sub-group into CRC group and cancers outside the gastrointestinal tract (COGT) group. Macroscopic and microscopic examinations were performed to identify intestinal parasites in participants’ stool samples. Molecular and phylogenetic analyses were conducted to identify and subtype Blastocystis. Furthermore, gut fungi were investigated molecularly. RESULTS: 104 stool samples were collected and matched between CF (n=52) and cancer patients (n=52); CRC (n=15) and COGT (n=37). As anticipated, Blastocystis prevalence was significantly higher among CRC patients (60%, P=0.002) and insignificant in COGT patients (32.4%, P=0.161) compared to CF group (17.3%). The most common subtypes were ST2 among cancer group and ST3 in the CF group. CONCLUSION: Cancer patients have a higher risk of Blastocystis infection compared to CF individuals (OR=2.98, P=0.022). Increased risk of Blastocystis infection was associated with CRC patients (OR=5.66, P=0.009). Nevertheless, further studies are required to understand the underlying mechanisms of Blastocystis and cancer association.
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spelling pubmed-99866232023-03-07 The associated risk of Blastocystis infection in cancer: A case control study Labania, Lena Zoughbor, Sumaya Ajab, Suad Olanda, Marie Shantour, Sulaiman N. M. Al Rasbi, Zakeya Front Oncol Oncology BACKGROUND: Blastocystis is an anaerobic intestinal protozoan. Nine Blastocystis subtypes (STs) were detected in humans. A subtype-dependent association between Blastocystis and different cancer types has been debated in many studies. Thus, this study aims to assess the possible association between Blastocystis infection and cancer, especially colorectal cancer (CRC). We also screened the presence of gut fungi and their association with Blastocystis. METHODS: We used a case-control design; cancer patients and cancer-free (CF) participants. The cancer group was further sub-group into CRC group and cancers outside the gastrointestinal tract (COGT) group. Macroscopic and microscopic examinations were performed to identify intestinal parasites in participants’ stool samples. Molecular and phylogenetic analyses were conducted to identify and subtype Blastocystis. Furthermore, gut fungi were investigated molecularly. RESULTS: 104 stool samples were collected and matched between CF (n=52) and cancer patients (n=52); CRC (n=15) and COGT (n=37). As anticipated, Blastocystis prevalence was significantly higher among CRC patients (60%, P=0.002) and insignificant in COGT patients (32.4%, P=0.161) compared to CF group (17.3%). The most common subtypes were ST2 among cancer group and ST3 in the CF group. CONCLUSION: Cancer patients have a higher risk of Blastocystis infection compared to CF individuals (OR=2.98, P=0.022). Increased risk of Blastocystis infection was associated with CRC patients (OR=5.66, P=0.009). Nevertheless, further studies are required to understand the underlying mechanisms of Blastocystis and cancer association. Frontiers Media S.A. 2023-02-20 /pmc/articles/PMC9986623/ /pubmed/36890816 http://dx.doi.org/10.3389/fonc.2023.1115835 Text en Copyright © 2023 Labania, Zoughbor, Ajab, Olanda, Shantour and Al Rasbi https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Labania, Lena
Zoughbor, Sumaya
Ajab, Suad
Olanda, Marie
Shantour, Sulaiman N. M.
Al Rasbi, Zakeya
The associated risk of Blastocystis infection in cancer: A case control study
title The associated risk of Blastocystis infection in cancer: A case control study
title_full The associated risk of Blastocystis infection in cancer: A case control study
title_fullStr The associated risk of Blastocystis infection in cancer: A case control study
title_full_unstemmed The associated risk of Blastocystis infection in cancer: A case control study
title_short The associated risk of Blastocystis infection in cancer: A case control study
title_sort associated risk of blastocystis infection in cancer: a case control study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986623/
https://www.ncbi.nlm.nih.gov/pubmed/36890816
http://dx.doi.org/10.3389/fonc.2023.1115835
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