Research Article |
Corresponding author: Putri Cahaya Situmorang ( putri.cahaya@usu.ac.id ) Academic editor: Georgi Momekov
© 2023 Putri Cahaya Situmorang, Rostime Hermayerni Simanullang, Rony Abdi Syahputra, Masta Melati Hutahaean, Hizkianta Sembiring, Lailatun Nisfa, Endang Ratna Sari.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Situmorang PC, Simanullang RH, Abdi Syahputra R, Hutahaean MM, Sembiring H, Nisfa L, Sari ER (2023) Histological analysis of TGFβ1 and VEGFR expression in cervical carcinoma treated with Rhodomyrtus tomentosa. Pharmacia 70(1): 217-223. https://doi.org/10.3897/pharmacia.70.e96811
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Cervical carcinoma is one of the most common malignant carcinomas around the world, including Indonesia. Rhodomyrtus tomentosa is an herbal medicine that is often used in Asia as a therapeutic agent to stop cancer metastases. The process of neoangiogenesis in cervical cancer depends on VEGFR activity. Increased TGFβ1 production is also linked to cervical cancer, suggesting that gene inactivation contributes to the emergence of cervical carcinoma.
Group C- was the control group, Group C+ was the cancer model group, CER100 was the group of rats with cancer + 100 mg/kg body weight (BW) of R. tomentosa, CER200 was the group of rats with cancer + 200 mg/kg BW of R. tomentosa, and CER400 was the group of rats with cancer + 400 mg/kg BW R. tomentosa. Rats were dissected after administration of R. tomentosa for 30 days. Immunohistochemical staining of the cervical tissue was performed with TGFβ1 and VEGFR antibodies. VEGFR expression was significantly different from TGFβ1 expression (p < 0.01). The highest expression was observed at the lowest dose of R. tomentosa (100 mg/kg BW), and the lowest expression was observed at 200 and 400 mg/kg BW. The administration of R. tomentosa can repair tissue damage and decrease the expression of TGFβ1 and VEGFR via histopathological parameters, indicating the importance of the activity of these proteins in the development of neoangiogenesis in cervical cancer.
cervical cancer, immunohistochemistry, molecular therapy, Rhodomyrtus tomentosa, TGFβ1, VEGFR
Cervical carcinoma of the uterus is one of the most prevalent malignant carcinomas that endangers the lives of women (
For tumour invasion and metastasis to occur in a mutually beneficial manner, vascular endothelial cell growth factor (VEGF) is required. Furthermore, there is a direct connection between angiogenesis and the development of the lymphatic system (
Transforming growth factor β1 (TGFβ1) can boost normal cervical remodelling and inhibit cervical cell growth induced by human papillomavirus (HPV) (
The findings of a study on VEGFR1 and TGFβ1 expression highlight the potential of R. tomentosa as a molecular therapy for cancer and provide strong support for its therapeutic use in modern medicine. The effect of R. tomentosa on VEGFR1 and TGFβ1 expression in rat cervical histopathology should be investigated before employing human cells. To increase cell penetration and bioavailability, R. tomentosa was formulated into a micro-colloidal form. It is intended to use this plant to produce drugs for human molecular cancer therapy.
R. tomentosa leaves were discovered in the Lintong Nihuta, North Sumatera, Indonesia. The plants were found in the Lintong Nihuta sub-district of Humbahas Regency at elevations ranging from 1,000 to 1,500 m above sea level and located at 02°4'20"–2°16'15"N and 98°52'40"–98°56'20"E. Lintong Nihuta District has 479 ha of peatland, accounting for 16.03% of the total peatland area in Humbang Hasundutan Regency (Hutagaol et al. 2021).
Preparation: The leaves and twigs of R. tomentosa were separated. The leaves were cleansed of any soil or dust that adhered to them, and they were dried for 7 days at room temperature and smoothed.
Extraction: 500 grams of R. tomentosa dry powder were macerated in 96% technical ethanol for 24 hours at room temperature. Maceration with a 96% technical ethanol solvent yielded the ethanol extract of R. tomentosa. The maceration products were filtered using a Buchner funnel and a vacuum pump. Using the same method, the filtered residue was macerated twice more. A rotary evaporator was used to concentrate the ethanol extract, which was then dried for 8 hours to produce a solid ethanol extract.
Production of micro-colloidal R. tomentosa (CER): An ethanol extract of the leaves was prepared by sonication as follows: 0.5 mg of R. tomentosa extract was added to a Tween 20 solution. Capryol 90 was added, and the solution was homogenised. PEG-400 was added, and the solution was sonicated. The prepared substance was dissolved in distilled water (1:100) and sonicated with an ultrasonic device (Sonicator Ultrasonic Homogenizers and Emulsifiers), and the micro-colloidal R. tomentosa was ready for use in animals experiments.
This study was conducted at the University of Sumatera Utara’s (USU) Biology, Pathology and Anatomy Laboratory of the Faculty of Medicine from January 2022 to August 2022. The study was conducted using a completely randomised design. This type of research is known as an experimental study. There were five groups: Group C- was the control group, Group C+ was the cancer model group, Group CER100 was the group of rats with cancer + 100 mg/kg body weight (BW) of R. tomentosa, Group CER200 was the group of rats with cancer + 200 mg/kg BW of R. tomentosa, and CER400 was the group of rats with cancer + 400 mg/kg BW R. tomentosa. R. tomentosa leaf ethanol extract was administered for 30 days orally. The animals were euthanized with administering an anaesthetic combination of 300 mg/kg BW of ketamine and 15–30 mg/kg BW of xylazine was administered then rats were dissected for taken the cervix and cervical tissues were stained with VEGFR1 and TGFβ1 antibodies using immunohistochemical techniques.
Thirty female Rattus norvegicus were used in this study. The rats were aged 10–15 weeks and weighed 180–200 g. Before being kept in cages at constant room temperature (25.0 ± 3.0 °C) and a humidity level of 35–60%, male rats were introduced to the laboratory environment for 2 weeks. The cages were lit for 12 hours and darkened for 12 hours. Female rats were given unrestricted access to water and free access to corn and pellets. Rats were placed in a plastic container measuring 40 cm × 30 cm. The rats were injected vaginally with 50 mg of benzopyrene diluted with corn oil. The tumour was identified when a lump was found due to administration of benzopyrene for three months, and samples were sent to the Anatomical Pathology Laboratory of the USU to ensure that the tissue was tumorous. The rats were then administered R. tomentosa for 1 month. The dose was in accordance with the acute toxicity test and previous studies (
Superoxide dismutase (SOD) analysis was performed using the blood of the rats with cervical cancer. The Superoxide Dismutase Activity Kit was used to measure SOD activity. After dilution with a uniquely coloured sample diluent, the sample is loaded into wells. Xanthine oxidase reagent was added after the substrate, and the mixture was allowed to sit at room temperature for 20 minutes. In the presence of oxygen, xanthine oxidase generates superoxide, which converts the colourless substrate in the detection reagent to a yellow product that is detectable at 450 nm.
Blood plasma samples from the rats were assessed with traditional thiobarbituric reactive species spectrophotometry (TBARS). The Malondialdehyde (MDA) Assay Kit (competitive enzyme-linked immunosorbent assay) (ab238537) was used for rapid detection and quantification of the protein MDA. This kit enables the quantification of MDA addition in a determined protein sample by comparing its absorbance with a known MDA-BSA standard curve. Then, the MDA-TBA2 condensation product can be measured via UV-VIS spectrophotometry.
Cervical organs were fixed in formalin and immersed in xylol for 15 minutes. After 5 minutes of alternating immersion in 96% and 70% pure alcohol, the tissues were washed with distilled water. After exposure to haematoxylin dye for 5 minutes, the tissues were washed in distilled water for 3 minutes, and the eosin stain was applied for 1 minute. Prior to immersion in xylol, the slides were dried in 70%, 96%, and 100% alcohol. Light microscopy analysis was then performed (
The histological changes in TGFβ1 and VEGFR expression in cervical carcinoma were investigated using immunohistochemistry after R. tomentosa leaf extract administration. The paraffin-fixed cervix samples were deparaffinised and treated for 30 minutes with 1% H2O2 in methanol to decrease endogenous peroxidase activity. The slides were then washed with 0.01 M Tris-buffered saline (pH 7.4). The tissue slices were treated with TGF-1 monoclonal antibody (catalogue #MA1-169 [B11-4C3]), VEGFR1 (soluble) polyclonal antibody (catalogue #36-1100), and Antigen Affinity-Purified Polyclonal Antibody (eBioscience Inc, San Diego, USA). The VECTASTAIN Elite ABC Kit (Vector Laboratories, USA) was used to detect immunoreactivity, which Mayer’s haematoxylin neutralised (
The Kruskal–Wallis and Mann–Whitney tests were performed on categorical (ordinal) or numerical data that were not normally distributed after data collection.
There was a significant difference in SOD levels between the C- and C+ groups based on ANOVA analysis with Bonferroni post hoc test (p < 0.05) (Table
There was a significant difference in MDA level between the C- and C+ groups based on ANOVA analysis with Bonferroni post hoc test (p < 0.05) (Table
According to the Kruskal–Wallis analysis, there was a significant difference (p = 0.000) (Table
Groups | Mean ± SD | Kruskal- Wallis | Mann-Whitney (p-value) | ||||
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C- | C+ | CER100 | CER200 | CER400 | |||
C- | 10.92 ± 1.02 | 0.000 | 0.0001 | 0.001 | 0.001 | 0.040 | |
C+ | 72.10 ± 8.22## | 0.030 | 0.010 | 0.001 | |||
CER100 | 49.09 ± 4.09* | 0.040 | 0.010 | ||||
CER200 | 24.67 ± 4.81** | 0.030 | |||||
CER400 | 19.07 ± 3.92** |
The cervical cells in group C- had histologically normal epithelial lining and nuclei (Fig.
TGF β1 expression of Cervical cancer after given Rhodomyrtus tomentosa, a. Control (C-); b. Cervical cancer (C+); c. Cervical cancer +100 mg/BW of Rhodomyrtus tomentosa (CER100); d. Cervical cancer + 200 mg/BW of Rhodomyrtus tomentosa (CER200); e. Cervical cancer + 400 mg/BW of Rhodomyrtus tomentosa (CER400). Red arrows: Positive expression. MF: Mucous folds, FLE: Flattened layered epithelium, ICT: Interstitial connective tissue (40X).
According to the Kruskal–Wallis test, there was a significant difference (p = 0.000) (Table
Groups | Mean ± SD | Kruskal- Wallis | Mann-Whitney (p-value) | ||||
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C- | C+ | CER100 | CER200 | CER400 | |||
C- | 5.18 ± 4.71 | 0.000 | 0.001 | 0.001 | 0.050 | 0.040 | |
C+ | 83.88 ± 6.55## | 0.070 | 0.040 | 0.020 | |||
CER100 | 70.22 ± 7.29ns | 0.040 | 0.040 | ||||
CER200 | 25.07 ± 7.09* | 0.040 | |||||
CER400 | 19.82 ± 4.02** |
Normal histological changes are shown in Fig.
VEGFR expression of Cervical cancer after given Rhodomyrtus tomentosa, a. Control (C-); b. Cervical cancer (C+); c. Cervical cancer +100 mg/BW of Rhodomyrtus tomentosa (CER100); d. Cervical cancer + 200 mg/BW of Rhodomyrtus tomentosa (CER200); e. Cervical cancer + 400 mg/BW of Rhodomyrtus tomentosa (CER400). Red arrows: Positive expression. MF: Mucous folds, FLE: Flattened layered epithelium, ICT: Interstitial connective tissue (40X).
Increased MDA and decreased SOD levels were observed in rates with cervical cancer (Tables
R. tomentosa, when administered in various doses, may decrease the prevalence of brown-stained nuclei, which are indicative of TGFβ1 expression in cancer tissue. The growth of the previously uncontrollable malignancy in the untreated group was slowed down and stopped in the epithelium. Immune cells of varying types and numbers can be detected in nests of tumour cells that are surrounded by different densities of intratumoral stroma in cervical cancer (Principe et al. 2014). TGFβ1 production is prevalent in women with cervical cancer (Principe et al. 2014; Taylor et al. 2021). TGFβ1 in cervical cancer reveals that gene inactivation contributes to cervical carcinoma development (
Cervical cancer development was halted at doses of 200 mg/kg BW to 400 mg/kg BW, indicating that this herb might be effective in suppressing VEGFR expression. An increase in VEGF expression in precancerous changes and cervical cancer is indicative of the role of this proangiogenic factor in the mechanism of neoangiogenesis (
The elevated expression of TGFβ1 and VEGFR in cervical carcinoma cells with poor histological characteristics shows how important these proteins’ actions are in the neoangiogenesis and progression of cervical cancer. R. tomentosa has been demonstrated to heal carcinogenic metastatic carcinoma tissue; it can be administered at various doses to decrease the number of brown nuclei that exhibit a positive index of TGFβ1 and VEGFR expression in cancer tissues.