<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sadowska A</submitter><funding>Medical University of Białystok</funding><funding>Bialystok University of Technology</funding><pagination>1352</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9919637</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(3)</volume><pubmed_abstract>Fungal extracts possess potential anticancer activity against many malignant neoplastic diseases. In this research, we focused on the evaluation of &lt;i>Heterobasidion annosum&lt;/i> (HA) extract in colorectal cancer in an in vivo model. The mice with implanted DLD-1 human cancer cells were given HA extract, the referential drug-5-fluorouracil (5FU), or were treated with its combination. Thereafter, tumor volume was measured and apoptotic proteins such as caspase-8, caspase-3, p53, Bcl-2, and survivin were analyzed in mice serum with an ELISA assay. The Ki-67 protein was assessed in tumor cells by immunohistochemical examination. The biggest volumes of tumors were confirmed in the DLD-1 group, while the lowest were observed in the population treated with 5FU and/or HA extract. The assessment of apoptosis showed increased concentrations of caspase 8 and p53 protein after the combined administration of 5FU and HA extract. The levels of survivin and Bcl-2 were decreased in all tested groups compared to the DLD-1 group. Moreover, we observed a positive reaction for Ki-67 protein in all tested groups. Our findings confirm the apoptotic effect of extract given alone or with 5FU. The obtained results are innovative and provide a basis for further research concerning the antitumor activity of the HA extract, especially in the range of its interaction with an anticancer chemotherapeutic agent.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Beneficial Proapoptotic Effect of Heterobasidion Annosum Extract in Colorectal Cancer Xenograft Mouse Model.</pubmed_title><pmcid>PMC9919637</pmcid><funding_grant_id>WZ/WB-INL/2/2021</funding_grant_id><funding_grant_id>SUB/3/DN/19/002/3327/2020</funding_grant_id><pubmed_authors>Sokolowska E</pubmed_authors><pubmed_authors>Car H</pubmed_authors><pubmed_authors>Sadowska A</pubmed_authors><pubmed_authors>Sawicka D</pubmed_authors><pubmed_authors>Guzinska-Ustymowicz K</pubmed_authors><pubmed_authors>Zapora E</pubmed_authors><pubmed_authors>Godlewska K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Beneficial Proapoptotic Effect of Heterobasidion Annosum Extract in Colorectal Cancer Xenograft Mouse Model.</name><description>Fungal extracts possess potential anticancer activity against many malignant neoplastic diseases. In this research, we focused on the evaluation of &lt;i>Heterobasidion annosum&lt;/i> (HA) extract in colorectal cancer in an in vivo model. The mice with implanted DLD-1 human cancer cells were given HA extract, the referential drug-5-fluorouracil (5FU), or were treated with its combination. Thereafter, tumor volume was measured and apoptotic proteins such as caspase-8, caspase-3, p53, Bcl-2, and survivin were analyzed in mice serum with an ELISA assay. The Ki-67 protein was assessed in tumor cells by immunohistochemical examination. The biggest volumes of tumors were confirmed in the DLD-1 group, while the lowest were observed in the population treated with 5FU and/or HA extract. The assessment of apoptosis showed increased concentrations of caspase 8 and p53 protein after the combined administration of 5FU and HA extract. The levels of survivin and Bcl-2 were decreased in all tested groups compared to the DLD-1 group. Moreover, we observed a positive reaction for Ki-67 protein in all tested groups. Our findings confirm the apoptotic effect of extract given alone or with 5FU. The obtained results are innovative and provide a basis for further research concerning the antitumor activity of the HA extract, especially in the range of its interaction with an anticancer chemotherapeutic agent.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-25T19:25:06.797Z</modification><creation>2025-04-06T07:57:04.27Z</creation></dates><accession>S-EPMC9919637</accession><cross_references><pubmed>36771018</pubmed><doi>10.3390/molecules28031352</doi></cross_references></HashMap>