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Chemical Content and Cytotoxic Activity on Various Cancer Cell Lines of Chaga (Inonotus obliquus) Growing on Betula pendula and Betula pubescens

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06 May 2024

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08 May 2024

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Abstract
Chaga (Inonotus obliquus) is a pathogenic fungus that grows mostly on birch species (Betula pendula and B. pubescens) and has traditionally been used as an anti-cancer medicine. The study aimed to compare the chemical composition and cytotoxic activity of chagas growing on both Betula spp. on various cancer cell lines. The freeze dried extracts contained triterpenes inotodiol, lanosterol betulin and betulinic acid typical to conks growing on Betula species. The cytotoxic activity of chaga growing on Betula pendula and B. pubescens 80% ethanolic extracts against thirty-one human cancer cell lines has been evaluated by a sulforhodamine B assay. The strongest inhibitions were observed with chaga (growing on B. pendula) extract on the HepG2 and CAL-62 cell line, and with chaga (from B. pubescens) extract on HepG2 cell line, with IC50 values of 37.71, 43.30, and 49.99 μg/mL, respectively. The chaga extracts from B. pendula exert somewhat stronger effects on most cancer cell lines studied than B. pubescens extracts. This study highlight the potential of chaga as a source of bioactive compounds with selective anti-cancer properties, encouraging further exploration of its therapeutic mechanisms and potential applications in cancer treatment.
Keywords: 
Subject: Medicine and Pharmacology  -   Pharmacy

1. Introduction

A basidiomycete fungus chaga (Inonotus obliquus) typically occurs on the trunks of trees growing in the Northern Hemisphere [1]. This pathogenic fungus grows mostly on birch species (Betula spp.) and is less known on other trees [2,3]. As a real parasite, chaga kills the host organism to fulfil its lifecycle [4]. Due to being found mainly on birch trunks, the chaga drug is known in pharmacy as Fungus betulinus, not to be confused with another species, e.g., Piptoporus betulinus.
As a natural source of biologically active substances, the chaga has been traditionally used as an anti-tomor, anti-inflammatory, antibacterial, hepatoprotective, and antioxidant natural remedy [5]. Chaga has been recognized for its medicinal uses since the sixteenth century [6]. Owing to containing a range of pharmaceutical and nutraceutical value, including polyphenols, triterpenoids, polysaccharides, and lignin, chaga has demonstrated diverse therapeutic effects. These encompass antioxidant, anti-inflammatory, antibacterial, antiviral, hepatoprotective, antidiabetic, anti-obesity, renoprotective, hepatoprotective, immunomodulatory, anti-tomor and anti-fatigue activities. Significantly, chaga has shown efficacy in anticancer activities [6,7,8].
The conks of I. obliquus have been the best known and most popular anti-cancer remedy in Estonian ethnomedicine among other 43 natural drugs [9]. Nowadays, chaga is rather well studied and primarily known as a promising natural material against cancer and for immunotherapy [10,11,12,13,14]. The anticancer activity of chaga has been studied by several researchers [11,15,16,17,18,19,20].
The aim of the study was to compare 1) chemical composition, and 2) cytotoxic activity of chagas growing on Betula pendula and B. pubescens on various cancer cell lines.
To the best of our knowledge, except for cytotoxic activity against HepG2 cell lines, the investigation of cytotoxicities against the tested cell lines of chaga parasitizing on B. pendula and B. pubescens for the first time.

2. Results

2.1. Phytochemical Study of Chaga

2.1.1. Extracts and Content of Biochemical Compounds

Freeze-dried ethanol extracts of chaga growing on two species, Betula pendula and B. pubescens, were prepared and analysed for triterpenoid composition and antioxidant activity (Table 1).
Although the ratio of dried raw material and solvent were the same for both samples the yield of freeze dried dry extract from samples differed slightly. 50 g of B. pendula conks resulted in 1.26 g of dry extract and the same amount of B. pubescens gave 1.45 g of dry extract.
There were no significant differences in the content of sitosterol and betulinic acid. Also antioxidant activity evaluated using DPPH method did not reveal any differences between these extracts (Table 1). Significant differences were revealed between the content of lanosterol, inotodiol and betulin in the extracts from conks from B. pubescens and B. pendula. The content of inotodiol in these samples was negatively correlated with the content of betulin and lanosterol, while betulin and lanosterol content had a strong positive correlation.

2.2. Cytotoxic Activity of Chaga

The cytotoxic activity of chaga (growing on B. pendula and B. pubescens) extract against thirty-one human cancer cell lines (Table 2) was evaluated by a sulforhodamine B assay [21,22]. The results of the cytotoxic assays are summarized in Table 3. These data showed that the strongest inhibitions were observed with chaga (growing on B. pendula) extract on the HepG2 and CAL-62 cell line and with chaga (growing on B. pubescens) extract on HepG2 cell line, with IC50 values of 37.71, 43.30, and 49.99 μg/mL, respectively. Chaga (growing on B. pendula) extract had no effect on NTERA-2, SK-LU-1, CL141, Huh-7R, NCI-N87, ACHN, AGS cancer cells (with IC50 values of > 100 μg/mL), and exhibited moderate inhibitory activity on other cell lines with IC50 values in the range of 55.29–97.73 μg/mL. Similarly, no activities were detected against MDA-MB-231, LNCaP, SK-LU-1, Hep3B, Huh-7, Huh-7R, MKN7, NCI-N87, AGS, SW626, SW480, HT29, ACHN, OCI/AML3 tested cell lines, and moderate cytotoxicities on the other cancer cell lines were observed with chaga (growing on B. pubescens) extract.

3. Discussion

The most abundant of the identified triterpenes was inotodiol as has been reported in the earlier studies [23]. The content of lanosterol, inotodiol and betulin varied between the extracts from B. pubescens and B. pendula significantly. Inotodiol content was higher in B. pendula extract and lanosterol and betulinic acid content in B. pubescens extracts. Correlation analysis revealed positive correlation between inotodiol content in the extract and the effect on growth inhibition on most of the tested cell lines. Negative correlation was revealed between inotodiol and growth inhibition only on cell lines NTERA-2 and 8505c.
Also, in previous study [4] the concentration of inotodiol was much more higher than other triterpenes lanosterol, betulin and betulinic acid. Upska et al. studied the extractability of chaga active ingredients using different methods and both polar and non-polar solvents. The best extractability of inotodiol was obtained by Soxhlet extraction using cyclohexane [24]. Inotodiol and lanosterol are both important compounds in chaga's anti-cancer effects [25,26]. Inotodiol and other lanostanes were effective against A549 cancer cells [27,28]. Inotodiol and lanosterol isolated from the conks of Betula spp. have immunological effect [13,29]. Inotodiol and lanosterol may also have cosmetic importance as they activate tyrosinase and increase pigment synthesis in skin cells [30]. Tian et al. showed that triterpenes of chaga may be an effective natural aid for treating and protecting various kidney diseases [31].
The antioxidant activity measurements performed using a DPPH assay showed same results for chaga from both Betula spp. The level of antioxidant activity may depend on the solvent used to extract chaga and the origin of the raw material. The difference in the DPPH scavenging activity may be up to 40 times different in chagas from various countries [10]. The scavenging activity of the water and ethanol extracts of chaga conks showed a similar level, but the methanol extract had the maximum IC50 values 18.96, 16.25, and 24.90 mg/mL, respectively [32].
In an earlier study [11], the methanol extract of chaga collected from the herb farm Kubja Ürditalu, Estonia, N59.054344, E25.963234, the commercial sample was purchased from a retail pharmacy in Tartu, Estonia, revealed potent cytotoxic effects against promyelocytic leukaemia and lung adenocarcinoma cells, with IC50 values of 32.2 and 38.0 µg/mL, respectively. Moreover, the extract showed moderate cytotoxicity (41.3–57.7 µg/mL) against cells from colon adenocarcinoma, liver hepatocellular carcinoma, oral epidermoid carcinoma, and prostate cancer [11]. This study assessed the anti-cancer properties of chaga (growing on B. pendula and B. pubescens) extracts across a diverse range of cancer cell lines. The results demonstrated a broad spectrum of cytotoxic effects, against 24 cancer cell lines for chaga (growing on B. pendula) extract including KB, MCF-7, LNCaP, A549, LLC, HepG2, Hep3B, HL-60, MKN7, SW626, Hela, SW480, RD, SK-Mel-2, OCI/AML3, K562, Jurkat, CAL-62, T24, Huh-7, HT29, 8505c, SNU1, MDA-MB-231, and against 17 cancer cell lines for chaga (growing on B. pubescens) extract including KB, MCF-7, CL141, A549, LLC, HepG2, HL-60, SNU1, Hela, RD, SK-Mel-2, K562, Jurkat, 8505c, CAL-62, T24, NTERA-2. Both chaga growing on these two host species possessed the most potential cytotoxic activities against HepG2 cell line, with IC50 values of 37.71 and 49.99 μg/mL, respectively. Furthermore, the extract of chaga (growing on B. pendula) exhibited remarkable cytotoxicity against the CAL-62 cell line, with an IC50 value of 43.30 μg/mL. Notably, liver cancer in men and thyroid cancer in women rank among the five most common types of cancer [20].
Here are some comparative data obtained using the same method in other natural products, which help to orient the strength of chaga's cytotoxic activity. The strongest anticancer effect of Matricaria chamomilla methanol extract against SK-MEL-2 cells was IC50 40.7 μg/mL, but the extract of Calendula officinalis showed weak cytotoxic activity against SK-MEL-2 and KB cells (IC50 62.6 and 79.2 μg/mL, respectively) [33]. The essential oils of Anthemis sylvestris roots and aerial parts had the strongest anticancer activity on KB cells (IC50 19.7 μg/mL and 19.8 μg/mL, respectively), while the methanolic extract had no effect [22]. The Pinus sylvestris needle methanol extract suppresses the viability of MDA-MB-231 cells on the level IC50 35 μg/mL [34]. In this context of anticancer activity, the effect of chaga’s extract, having the strongest values between 37.7-43.3 μg/mL, showed remarkable but not strong effects.
Chaga has received considerable attention from many researchers due to its numerous biological attributes, particularly its potential anticancer effects. According to Ma et al., the petroleum ether and ethyl acetate extracts of chaga displayed significant cytotoxic activities against the human prostatic carcinoma cell PC3 and breast carcinoma cell MDA-MB-231 [15]. The inhibitory effects were mainly attributed to ergosterol peroxide and trametenolic acid [15]. The aqueous extract of chaga in France containing a high content of betulin and betulinic acid and inotodiol showed an effect on human lung adenocarcinoma cells [18]. Noticeably, chaga extract was reported to markedly reduce HepG2 cell viability due to G0/G1-phase arrest and apoptotic cell death, thus leading to down-regulation of p53, pRb, p27, cyclins D1, D2, E, cyclin-dependent kinase (Cdk) 2, Cdk4, and Cdk6 expression [35]. Through matrigel-coated filters, the methanolic extract and its EtOAc-soluble fraction from Chaga collected in Japan showed the significant invasion inhibition of human fibrosarcoma HT 1080 cells. Importantly, compound 3β-hydroxylanosta-8,24-dien-21-al exhibited a strong inhibitory effect on HT 1080 cells. Furthermore, the methanolic extract of this sample significantly suppressed the formation of lung tomors in mice at 500 mg/kg/d [17]. The methanolic extract of Russian chaga purchased in Korea showed inhibitory effects toward four human lung adenocarcinoma cell lines (including A549, H1264, H1299, and Calu-6) through induction of apoptosis accompanied by caspase-3 cleavage. Significantly, compounds 3β-hydroxylanosta-8,24-dien-21-al, trametenolic acid, and 3β-hydroxy-5αlanosta-8,25-dien-21-oic acid isolated from this extract showed cytotoxicities against these cell lines, with IC50 values ranging from 75.1 to 227.4 μM in the same pattern [36]. The aqueous extract of chaga (in Korea) displayed anti-proliferative activity on HCT116 and DLDl cell lines, and reduced in intestinal polyps in APCMin/+ and colon tomors in AOM/DSS-treated mice through downregulation of Wnt/β-catenin and NF- κB pathways [37]. The extract of chaga collected from birch trees in Japan successfully reduced tomors in both tomor-bearing mice and metastatic mice by promoting energy metabolism [16]. Additionally, the administration of chaga obtained in Japan could induce necrotic lesions, resulting in a decrease in the growth of the tomor and the weight of dog bladder cancer organoid-derived xenografts [19].
Current work and some others [4,11] indicate that Inonotus obliquus origin and the fungus host affects the source of useful bioactive compounds. Inonotus obliquus grows naturally on Betula spp. and on Alnus spp. as well as some other broadleaved trees in northern Baltic conditions [2,3]. In this area, the fungus grows on B. pendula and B. pubescens [2,3,38], and B. pendula is widely known host to the chaga [4], but not B. pubescens. However, nothing is known about the bioactive compounds of the chaga growing on B. pubescens. Current work shows evidently that the. bioactive compounds of chaga differ significantly according to the origin of quite close host species as B. pendula and B. pubescens. It indicates that the fungus origin and background are important for further analyses including effects on different human cancer cell lines.
These findings highlight the potential of chaga as a source of bioactive compounds with selective anti-cancer properties, encouraging further exploration of its therapeutic mechanisms and potential applications in cancer treatment.

4. Materials and Methods

4.1. Sample Sites, Fungal Isolation, Detection and Preparation

The conks of I. obliquus were collected from B. pendula and B. pubescens originate from Estonia between 21.12.2019 and 03.02.2022 (Table 4). The isolates were optained from fresh conks to grow on 2% malt-extract agar (Biolife, Milano, Italy) plates.
The DNA of I. obliquus isolates were extracted using a GeneJET Genomic DNA Purification Kit (Thermo Scientific, Vilnius, Lithuania) and the fungus was detected as described by Drenkhan et al. [39]. ITS-PCR products from the isolates were sequenced at the Estonian Biocentre in Tartu. The ITS sequences were edited using the BioEdit program, Version 7.2.5 [40] and deposited in a Genbank (see Table 4). BLAST searches for the fungal taxa confirmation were performed in the GenBank database (NCBI). All the pure cultures were deposited to the Fungal Culture Collection (TFC) and GenBank (NCBI).
Before extractions and biochemical analysis, the conks were kept in a freezer at -20 °C. Then, the collected conks were dried in a laboratory oven (MMM Medcenter Einrichtungen GmbH, Planegg, Germany) at 50 °C, and all the material was ground to a coarse powder using a cutting mill Retch SM 300 with a 1 mm sieve (Retsch, Haan, Germany). Extracts were prepared from the mix of 10 individual conks samples per host species in equal proportions (see Table 4). For extract preparation 500ml of 80% ethanol was added to 50g of dried and milled sample and agitated at room temperature for 12 hours using Biosan ES20 orbital shaker. After vacuum filtration, the extracts were concentrated on rotary evaporator RV 10 control Flex (IKA-Werke GmbH & Co. KG. Germany) to remove most of the ethanol and further dried in the freeze-drier VirTis AdVantage 2.0 EL (SP Scietific, USA). Bioactive compounds detection from I. obliquus was done according to [4].
Antioxidant activity measurements were performed in triplicate using a 2.2-diphenyl-picrylhydrazyl (DPPH) assay [41]. The absorbance values of the samples were measured at 515 nm using a spectrophotometer (UV-1800, Shimadzu, Japan). The results were expressed in mg of gallic acid equivalent per g of dry weight (mg GA eq./g).
Qualitative and quantitative analyses were performed on a Shimadzu Nexera X2 UHPLC with mass spectrometer LCMS 8040 (Shimadzu Scientific Instruments, Kyoto, Japan). The UHPLC system was equipped with a binary solvent delivery pump LC-30AD, an autosampler Sil-30AC, column oven CTO-20AC and diode array detector SPD-M20A. Five triterpenoids (betulinic acid, betulin, lanosterol, inotodiol and sitosterol) were identified by comparing the retention times and parent and daughter ion masses with those of the standard compounds. Chromatographic separation was performed using Ascentis Express column (C30 50 x 4,6mm, Merck, Germany ) at 40 °C. The flow rate of the mobile phase was 1 mL/min, and the injected sample size was 1 µL. Mobile phases consisted of 1% formic acid in Milli-Q water (mobile phase A) and 1% formic acid in acetonitrile (mobile phase B). Separation was performed for 10 min at isocratic conditions with 92% of mobile phase B and 8% of mobile phase A. All samples were kept at 4 °C during the analysis. MS data acquisitions were performed on LCMS 8040 with the APCI source. All samples were analysed in triplicate, and the results were expressed as mg per g of dry weight (mg/g).
The standards betulin, betulinic acid and lanosterol were purchased from Cayman Chemical Company (USA) and inotodiol from Aobious (USA). All other standards (sitosterol, gallic acid) and chemicals (formic acid, methanol) were used of analytical grade and purchased from Sigma (Germany).
The dry matter content in the samples was determined at 105 °C using moisture analyser Precisa EM 120 HR (Precisa Gravimetrics AG, Switzerland).

4.2. Cytotoxic Assay

A total of 31 human cancer cell lines (Table 1 and Table 2) were cultivated at 37 °C in a humidified atmosphere containing 5% carbon dioxide. SRB cytotoxic assay for monolayer cells has been analyzed according to the method described in [42,43,44].
The 80% ethanolic dry extracts were firstly stocked in dimethyl sulfoxide (DMSO) 100% at the concentration as 20 mg/mL. The samples were then prepared in a range of diluted concentrations as 2000 µg/mL - 400 µg/mL - 80 µg/mL - 16 µg/mL using basic RPMI medium (w/o FBS) in 96 sample plate. Then, 10 µL from each well (with the diluted sample above) will be added into the tested cell pre-seeded (190 µL) well to evaluate cytotoxic activities. Thus, the final concentration of the sample will be 100 µg/mL - 20 µg/mL - 4 µg/mL - 0.8 µg/mL. Ellipticine was tested with the final concentration ranging as 20-4-0.8-0.16 µg/mL.
The effects of Betula chaga hydroethanolic extracts on the viability of malignant cells were determined by sulforhodamine B cytotoxic assay [43,44]. Briefly, cells were grown in 96-well microtiter plates, each containing 190 μL of medium. After 24 h, 10 μL of test samples dissolved in DMSO were added to each well. One plate with no samples served as a day 0 control. The cells were continuously cultured for an additional 48 h, fixed with trichloroacetic acid, and stained with sulforhodamine B, followed by determining optical densities at 515 nm using a Microplate Reader (BioRad, California, USA). The percentage of growth inhibition was calculated using the following equation:
[OD (reagent) - OD (day 0)] ×100
   % Growth =
   [OD (negative control DMSO 10%) - OD (day 0)],
where OD is the optical density or absorbance values. The potent anticancer agent ellipticine was used as a positive control.

4.4. Statistics

Biochemical analysis data were analysed using Jamovi software [45]. Metabolite concentrations were analysed by one-way analysis of variance (ANOVA). Differences between means were assessed with Post Hoc Tukey test. The IC50 values were analyzed using TableCurve 2Dv4 software.

5. Conclusions

The strongest inhibitions were observed with both hosts (Betula pendula and B. pubescens) based chaga extracts on the HepG2 cell line. In general, the cytotoxic activity of chaga extracts has been at a moderate or weak level.
The B. pendula origin chaga extracts exert somewhat stronger effects on most cancer cell lines studied than B. pubescens parasitizing chaga extracts. This effect can be attributed to higher content of inotodiol in B. pendula origin extracts in comparison to B. pubescens. This is also the first comparative investigation of the chemical composition of I. obliquus parasitizing on B. pendula and B. pubescens.
The results of the study highlight the potential of chaga as a source of bioactive compounds with selective anti-cancer properties, encouraging further exploration of its therapeutic mechanisms and potential applications in cancer treatment.

Author Contributions

Conceptualization, A.R., H.K., O.K., H.T.N., and H.K; methodology, A.R., R.D., H.K., K.V.N. and H.T.N.; software, H.K..; validation, H.K., U.B. and K.V.N.; formal analysis, H.K., A.R.,A.A., and K.V.N.; investigation, H.K., U.B., M.S., K.A., A.A., M.E., and K.K.; resources, M.S., K.A., K.K., M.V., A.A., and M.E.; data curation, K.J., H.K., A.R., O.K., H.T.N. and R.D.; writing—original draft preparation, A.R., H.K., K.V.N., H.T.N., O.K., M.S. and R.D.; writing—review and editing, A.R., O.K. and R.D.; visualization, H.K., U.B. and A.R.; supervision, R.D., H.T.N. and A.R..; project administration, R.D., H.K., and A.R.; funding acquisition, R.D. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Inopure OÜ, Estonian University of Life Sciences project PM220078MIME, the Estonian Research Council, Grant PRG1615 and the European Regional Development Fund’s project “PlantValor—full-scale product development service in synergy with the traditional activities of Polli Horticultural Research Centre“ 2014-2020.5.04.19-0373.

Acknowledgments

The research was conducted using the „Plant Biology Infrastructure – TAIM“ funded by the Estonian Research Council (TT5).

Conflicts of Interest

The authors declare no conflict of interest.

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Table 1. The average content of triterpenoids and antioxidant activity of freeze dried extracts of chaga conks growing on Betula pendula and B. pubescens.
Table 1. The average content of triterpenoids and antioxidant activity of freeze dried extracts of chaga conks growing on Betula pendula and B. pubescens.
Antioxidant activity Triterpenoids Species
Aox GA eq 1 mg/g Sitosterol mg/g Lanosterol mg/g Betulin mg/g Betulinic acid mg/g Inotodiol mg/g
21.5±0.065 0.780±0.149 8.89±0.497a 7.22±0.104a 2.77±0.165 169±6.60a B. pendula
dry extract
21.4±0.045 0.770±0.0964 11.1±0.364ab 14.9±0.690b 2.05±0.476 149±2.30b B.pubescens dry extract
All values are given per g of freeze dried extract. All values are means ± standard deviation (n = 3); mean values within a column marked with different letters (a,b) are significantly different at p < 0.05. Differences between means were assessed with ANOVA and Post Hoc Tukey test. 1 Aox GA eq. mg/g antioxidant activity expressed as Gallic acid equivalent mg/g
Table 2. Abbreviations of 31 human cancerous cell lines.
Table 2. Abbreviations of 31 human cancerous cell lines.
Basic characteristics Name
Human carcinoma in the mouth KB
Human breast adenocarcinoma MDA-MB-231
Human breast carcinoma MCF7
Human prostate carcinoma LNCaP
Human lung carcinoma SK-LU-1
Human lung adenocarcinoma CL141
Human lung carcinoma A549
Lewis lung carcinoma - high metastasis LLC
Human hepatocellular carcinoma HepG2
Human hepatocellular carcinoma Hep3B
Human hepatocyte-derived carcinoma Huh7
Drug resistant human hepatocyte-derived carcinoma Huh 7R
Human acute leukemia HL-60
Human differentiated human gastric adenocarcinoma MKN7
Human gastric carcinoma NCI-N87
Human gastric adenocarcinoma AGS
Human stomach carcinoma SNU-1
Human ovarian adenocarcinoma SW626
Human cervix carcinoma Hela
Human colon adenocarcinoma SW480
Human colorectal adenocarcinoma HT-29
Human rhabdomyosarcoma RD
Human malignant melanoma SK-Mel-2
Human kidney adenocarcinoma ACHN
Human acute myeloid leukemia OCI/AML3
Human chronic myelogenous leukemia K562
Human acute T cell leukemia Jurkat
Human undifferentiated thyroid carcinoma 8505c
Human thyroid anaplastic carcinoma CAL-62
Human urine bladder carcinoma T24
Pluripotent human embryonal carcinoma NTERA2
Table 3. Cytotoxic activity of chaga extracts on various cancer cell lines.
Table 3. Cytotoxic activity of chaga extracts on various cancer cell lines.
Cancer cells’s line Concentration (µg/mL) Growth inhibition, %
Betula pendula Betula pubescens Ellipticine
Average SD Average SD Average SD
KB 100 69.38 1.12 90.50 2.86 90.50 2.86
20 20.49 1.65 70.14 1.96 70.14 1.96
4 6.88 0.42 65.56 1.60 65.56 1.60
0.8 -1.11 0.12 16.65 1.02 16.65 1.02
IC50 63.35±2.89 74.90±1.38 0.49±0.03
MCF-7 100 56.34 2.08 53.92 2.04 90.55 3.21
20 26.76 1.50 15.24 1.16 83.67 1.44
4 12.11 1.19 5.27 1.15 53.23 1.08
0.8 7.55 0.36 1.36 0.23 19.33 0.97
IC50 77.92±4.49 90.87±3.82 0.61±0.05
MDA-MB-231 100 51.21 2.15 45.24 1.01 90.55 3.21
20 12.79 1.01 14.74 0.63 83.67 1.44
4 10.43 0.96 1.59 0.14 53.23 1.08
0.8 4.33 0.14 -3.78 0.22 19.33 0.97
IC50 97.73±3.78 >100 0.68±0.07
LNCaP 100 60.19 1.36 46.39 2.31 97.83 4.44
20 26.13 0.78 12.97 1.13 80.77 1.51
4 12.42 1.19 9.13 0.24 58.59 1.92
0.8 6.63 0.51 1.54 0.12 31.77 1.42
IC50 70.46±2.17 >100 0.44±0.04
SK-LU-1 100 43.08 1.59 28.57 1.82 97.72 2.28
20 12.17 1.04 10.90 1.03 92.29 2.51
4 5.35 0.13 -0.15 0.02 65.40 1.57
0.8 0.74 0.04 -2.26 0.11 13.09 0.66
IC50 >100 >100 0.45±0.05
CL141 100 46.10 1.37 53.20 2.52 98.79 1.56
20 21.59 1.73 12.33 1.05 85.23 1.34
4 4.39 0.37 -1.53 0.17 61.63 1.08
0.8 1.72 0.12 -2.77 0.21 14.49 1.06
IC50 >100 92.81±4.55 0.55±0.03
A549 100 54.11 2.07 57.18 1.31 89.70 2.90
20 24.85 1.18 22.49 0.75 69.97 1.19
4 12.96 0.83 5.52 0.56 53.98 1.10
0.8 7.56 0.56 -0.94 0.05 25.15 1.04
IC50 85.44±5.27 78.32±3.31 0.62±0.04
LLC 100 80.74 3.19 76.82 1.63 100.26 3.92
20 23.07 1.78 22.49 1.06 90.22 2.18
4 8.68 0.55 13.33 0.39 73.21 1.96
0.8 -0.95 0.09 2.03 0.57 24.77 1.32
IC50 52.29±3.57 55.89±2.37 0.35±0.03
HepG2 100 90.94 3.13 85.96 3.13 91.65 3.42
20 31.91 1.26 24.65 1.63 83.80 2.45
4 17.16 1.06 5.60 0.56 69.66 1.39
0.8 2.74 0.23 4.65 0.53 26.16 1.06
IC50 37.71±2.08 49.99±1.94 0.37±0.02
Hep3B 100 60.78 1.46 45.95 1.73 99.31 1.76
20 17.38 1.40 17.92 0.80 82.09 2.26
4 5.93 0.13 4.66 0.53 53.19 1.03
0.8 -1.11 0.12 -3.92 0.28 18.23 1.92
IC50 76.70±3.42 >100 0.73±0.04
Huh-7 100 52.24 1.34 43.02 1.75 98.82 2.42
20 10.47 1.92 10.48 0.57 84.41 2.98
4 2.55 1.96 -2.34 0.23 57.02 1.77
0.8 -3.78 0.36 -4.14 0.31 16.32 1.03
IC50 95.34±3.36 >100 0.56±0.05
Huh-7R 100 42.81 0.85 39.22 2.27 96.45 2.40
20 13.62 1.01 6.67 0.40 82.09 1.21
4 0.35 0.03 4.16 1.80 51.64 1.28
0.8 -2.77 0.19 -0.56 0.03 18.18 1.52
IC50 >100 >100 0.66±0.06
HL-60 100 64.65 1.87 71.73 1.74 82.15 3.43
20 10.24 1.09 12.01 1.06 80.94 1.25
4 0.60 0.04 0.67 0.08 54.42 1.83
0.8 -1.59 0.12 -1.66 0.11 20.25 1.19
IC50 79.02±2.82 71.21±2.41 0.64±0.05
MKN7 100 69.44 2.80 47.07 2.80 95.10 2.15
20 15.72 1.54 11.74 0.69 91.13 1.57
4 5.45 0.21 5.63 0.26 64.56 1.00
0.8 -1.47 0.10 0.36 0.02 32.41 1.59
IC50 68.85±4.06 >100 0.36±0.02
NCI-N87 100 47.57 1.10 35.08 2.73 85.64 2.98
20 12.68 1.29 15.63 1.15 79.12 1.42
4 7.82 0.36 0.98 0.03 51.92 1.76
0.8 2.18 0.17 -1.11 0.12 16.90 1.33
IC50 >100 >100 0.75±0.06
AGS 100 46.35 2.10 34.89 2.10 92.21 3.67
20 13.34 0.63 13.69 1.47 81.27 1.32
4 2.09 0.17 2.95 0.26 52.92 1.42
0.8 -3.48 0.26 -2.66 0.12 21.04 0.54
IC50 >100 >100 0.68±0.03
SNU1 100 52.32 1.70 51.02 1.59 94.73 3.70
20 8.62 0.58 16.76 1.32 92.96 2.35
4 0.79 0.08 4.42 0.48 67.30 1.81
0.8 -1.56 0.13 0.97 0.05 20.36 1.40
IC50 95.82±2.97 97.02±4.61 0.44±0.02
SW626 100 55.52 2.13 46.25 2.79 100.09 2.13
20 21.43 1.58 10.00 1.32 92.09 2.51
4 2.90 0.25 6.11 1.78 61.96 1.40
0.8 -1.69 0.13 1.23 0.12 22.17 0.86
IC50 82.88±5.84 >100 0.51±0.03
Hela 100 62.80 1.86 51.56 1.66 98.00 2.00
20 23.77 0.95 19.53 0.88 97.00 1.09
4 6.12 0.12 2.12 1.14 61.55 2.61
0.8 1.89 0.16 -2.69 0.23 18.85 1.53
IC50 68.50±3.45 94.28±4.69 0.50±0.04
SW480 100 53.84 1.62 45.25 2.71 96.33 2.91
20 22.61 1.17 18.19 1.94 88.79 1.14
4 10.23 1.02 4.07 0.36 55.73 1.50
0.8 3.66 0.23 2.22 0.19 25.32 0.87
IC50 87.10±5.19 >100 0.53±0.02
HT29 100 56.32 1.74 45.71 2.24 95.82 2.67
20 15.85 1.38 26.46 0.73 93.62 1.72
4 5.88 0.46 13.07 1.10 66.36 1.87
0.8 1.66 0.12 5.15 0.28 30.68 1.59
IC50 86.08±6.03 >100 0.37±0.03
RD 100 56.70 2.83 62.14 2.69 92.16 1.76
20 17.47 1.43 10.09 1.25 79.32 1.45
4 5.02 0.56 2.59 0.21 45.26 1.20
0.8 1.33 0.11 -0.91 0.05 22.54 0.82
IC50 84.12±5.95 82.08±3.96 0.74±0.02
SK-Mel-2 100 66.82 1.98 63.12 2.67 97.00 4.08
20 24.41 1.06 20.91 1.34 95.90 2.33
4 6.55 0.65 4.15 0.13 61.23 1.36
0.8 1.87 0.12 1.22 0.10 14.20 0.56
IC50 62.82±3.20 71.18±4.61 0.57±0.02
ACHN 100 46.83 2.35 39.18 1.33 84.62 2.85
20 15.76 1.00 15.13 1.00 71.59 2.94
4 5.19 0.34 7.18 0.67 52.21 1.06
0.8 1.63 0.18 -1.69 0.12 18.95 1.12
IC50 >100 >100 0.77±0.02
OCI/AML3 100 59.86 1.15 34.58 1.86 85.35 1.15
20 35.60 1.73 27.65 1.29 84.74 1.44
4 20.31 1.29 14.80 1.17 54.36 1.03
0.8 8.64 0.65 4.69 0.24 24.32 1.25
IC50 55.57±4.33 >100 0.57±0.03
K562 100 77.43 2.43 65.77 1.96 91.72 2.15
20 19.91 1.38 16.59 1.01 81.50 1.23
4 10.24 1.02 10.34 0.91 65.13 2.14
0.8 5.36 0.25 5.64 0.34 20.50 0.81
IC50 61.41±3.28 75.00±3.17 0.46±0.04
Jurkat 100 69.35 2.14 66.17 1.99 91.26 1.07
20 22.01 1.11 10.84 1.07 81.23 0.46
4 7.45 0.54 1.33 0.77 52.63 1.84
0.8 2.94 0.13 -3.56 0.22 21.02 1.11
IC50 63.48±3.15 76.16±2.88 0.68±0.05
8505c 100 54.91 1.11 41.47 3.19 101.87 1.24
20 11.08 0.90 11.15 1.06 73.65 0.52
4 5.09 0.51 2.54 0.39 53.80 2.47
0.8 1.94 0.15 -1.74 0.16 19.73 1.84
IC50 91.50±1.80 69.42±3.10 0.59±0.02
CAL-62 100 73.84 1.82 66.49 1.61 80.96 1.63
20 35.08 1.22 17.63 1.43 71.77 1.84
4 15.03 1.02 2.86 0.18 52.56 1.03
0.8 6.87 0.35 -2.22 0.21 26.94 0.97
IC50 43.30±2.52 69.42±3.10 0.59±0.02
T24 100 61.17 2.41 52.46 3.90 92.74 1.77
20 18.11 1.58 13.94 1.00 87.92 1.07
4 5.08 0.53 0.22 0.02 57.97 1.16
0.8 1.93 0.15 -2.95 0.26 18.12 1.24
IC50 76.76±4.71 93.81±5.66 0.54±0.02
NTERA-2 100 40.10 2.37 65.20 2.52 96.98 1.82
20 21.59 1.73 18.33 1.35 95.23 0.34
4 4.39 0.37 -1.53 0.17 61.63 1.38
0.8 -4.71 0.24 -3.75 0.41 13.49 1.36
IC50 >100 70.11±3.93 0.57±0.03
Table 4. Origin and hosts of Inonotus obliquus, isolated from the conks and used in this study’s fungal strains.
Table 4. Origin and hosts of Inonotus obliquus, isolated from the conks and used in this study’s fungal strains.
Accsession no in GenBank** Fungal Collection code* Accsession no in GenBank** Sampling date Geographical coordinates Host Strain no
OP019325 TFC101258 OP019325 21.12.2019 N58.90373, E26.44672 Betula pendula PAT29045
OP942253 TFC101271 OP942253 30.12.2019 N58.06711, E26.42738 Betula pendula PAT29055
PP346417 TFC101304 PP346417 11.02.2020 N58.2567, E26.6659 Betula pendula PAT29051
OP942256 TFC101274 OP942256 09.11.2021 N58.52718, E22.91413 Betula pendula PATKA880
OP942259 TFC101277 OP942259 11.11.2021 N58.91147, E22.35235 Betula pendula PATKA896
OP942263 TFC101281 OP942263 27.01.2022 N57.82154, E27.48639 Betula pendula PATKA1567
OP942264 TFC101282 OP942264 27.01.2022 N57.82154, E27.48639 Betula pendula PATKA1568
OP942268 TFC101286 OP942268 25.01.2022 N59.01350, E27.60455 Betula pendula PATKA1575
OP942272 TFC101290 OP942272 03.02.2022 N59.27381, E25.36868 Betula pendula PATKA1679
OP942273 TFC101291 OP942273 03.02.2022 N59.27381, E25.36868 Betula pendula PATKA1680
OP942269 TFC101287 OP942269 25.01.2022 N59.01654, E27.44207 Betula pubescens PATKA1576
OP942270 TFC101288 OP942270 25.01.2022 N59.01367, E27.53098 Betula pubescens PATKA1577
OP942260 TFC101278 OP942260 11.11.2021 N58.98419, E22.72165 Betula pubescens PATKA900
PP346418 TFC101305 PP346418 17.10.2020 N58.9065, E26.0808 Betula pubescens PATRD3354
PP346419 TFC101306 PP346419 29.10.2020 N58.3203, E25.7080 Betula pubescens PATRD3364
PP346420 TFC101307 PP346420 05.03.2021 N58.3776, E25.9267 Betula pubescens PATRD3402
- TFC101308 - 15.03.2021 N58.9566, E25.4320 Betula pubescens PATRD3355_1
PP346421 TFC101309 PP346421 27.10.2021 N58.6825, E25.6854 Betula pubescens PATRD3356
PP346422 TFC101310 PP346422 17.12.2021 N59.4096, E26.6767 Betula pubescens PATRD3386
PP346423 TFC101311 PP346423 17.12.2021 N59.4932, E26.5887 Betula pubescens PATRD3385
* Tartu Fungal Collection in Estonian University of Life Sciences, Estonia (TFC). **ITS sequences in GenBank (NCBI).
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