Abstract
Breast cancer is a type
of cancer that originates in the cells of the breast tissues. B. pinnatum,
C. sieberiana, C. tora and T. indica are the four medicinal plants whose
phytochemicals were used for this In silico study. In this study, eight
different ligands were evaluated for their interactions with the human
epidermal growth factor 2 (HER2) protein (PDB ID: 3pp0). The ligands, including
Apigenin, Bryophyllin A, Catechin, Emodin, Islandicin, Quercetin, Sitosterol,
and Taxifolin, were assessed based on binding scores and hydrogen bond
interactions. Among these ligands, Apigenin exhibited the highest binding score
(- 6.5 kcal/mol), indicating its strong binding affinity to the HER2 protein.
Bryophyllin A also displayed a significant binding score (- 6.3 kcal/mol) and
formed a hydrogen bond with Met 901. Catechin, while having a slightly lower
binding score (- 5.9 kcal/mol), engaged in hydrogen bonds with Ser 728, Arg
849, and Asn 850. Emodin, Quercetin, and Taxifolin demonstrated moderate
binding scores (- 6.2, – 6.4, and – 6.0 kcal/mol, respectively) and formed
hydrogen bonds with Asp 863 and Met 801. Islandicin formed a hydrogen bond with
Gly 787 and Leu 786, with a binding score of – 6.1 kcal/mol. Sitosterol
exhibited the lowest binding score (- 5.3 kcal/mol) but still established a
hydrogen bond with Asp 863 and Met 801. Overall, Apigenin and Bryophyllin A
emerged as the most promising ligands due to their strong binding affinities
and specific hydrogen bond interactions with HER2. However, experimental
validation is essential to confirm these findings and explore their potential
as inhibitors or modulators of HER2. Furthermore, all ligands were successfully
docked to the active sites of the HER2 protein, indicating their potential
relevance in targeting HER2-related pathways. Importantly, the ligands
exhibited favorable pharmacokinetic properties with no violations, except for
Sitosterol, which showed minor violations in Lipinski, Ghose, Egan, and Muegge’s
rules.
Introduction
Breast cancer is a type of cancer that originates in the cells of the breast tissues. It primarily affects women but can also occur in men. It is characterized by the uncontrolled growth of abnormal cells in the breast tissue, forming a lump or mass called a tumor (Dashti et al., 2020). Breast cancer can spread to other parts of the body through the lymphatic system or bloodstream, leading to metastasis (Iqbal and Iqbal, 2014; Pegram and Jackisch, 2023). Early detection and advancements in treatment have significantly improved the prognosis and survival rates for those diagnosed with breast cancer (Pegram and Jackisch, 2023). The exact causes of breast cancer are not fully understood, but several risk factors have been identified. These include genetics (family history of breast cancer or carrying certain mutations like BRCA1 and BRCA2), hormonal factors (early onset of menstruation, late menopause, hormone replacement therapy), age (risk increases with age), certain inherited gene mutations, exposure to ionizing radiation, obesity, alcohol consumption, and more (Sun et al., 2017). While these factors can increase the risk, not everyone with these risk factors will develop breast cancer. Breast cancer can have wide-ranging effects on individuals physically, emotionally, and socially. Physically, it can lead to symptoms such as a lump in the breast, changes in breast size or shape, skin changes, and nipple discharge (Kim, 2021; Sun et al., 2017). Emotionally, the diagnosis can cause anxiety, fear, depression, and uncertainty. Socially, it may impact relationships and daily life. The effects of treatment, including surgery, chemotherapy, radiation, and hormone therapy, can also cause physical and emotional challenges. Treatment for breast cancer depends on the stage and type of cancer, as well as individual factors (Iqbal and Iqbal, 2014; Pegram and Jackisch, 2023). Common treatments include surgery (lumpectomy or mastectomy), radiation therapy, chemotherapy, targeted therapy, hormone therapy, and immunotherapy (Burguin and Diorio, 2021; Moo et al., 2019). Treatment plans may involve a combination of these approaches (Pegram and Jackisch, 2023). The goal is to remove or destroy the cancer cells, prevent recurrence, and improve overall quality of life (Moo et al., 2019). Researchers have identified specific molecular and genetic targets that play a role in the development and growth of breast cancer. Targeted therapies focus on these specific molecules, receptors, and genetic mutations to inhibit cancer growth (Burguin and Diorio, 2021). Some targeted therapies are designed to block hormone receptors (such as estrogen or progesterone receptors), while others target overexpressed proteins like HER2. HER2, or human epidermal growth factor receptor 2, is a protein that plays a role in regulating cell growth and division. In some breast cancers, there is an overexpression or amplification of the HER2 gene, leading to an increased production of the HER2 protein (Hussain et al., 2020; Iqbal and Iqbal, 2014). HER2-positive breast cancer is an important target in breast cancer treatment because the overexpression of HER2 is associated with more aggressive tumor growth and a poorer prognosis (Iqbal and Iqbal, 2014). Targeting HER2 can help slow down the progression of the cancer and improve treatment outcomes. In molecular docking studies, the HER2 (human epidermal growth factor receptor 2) protein is commonly used as a target protein, especially when investigating the binding of potential drug compounds or ligands (Iqbal and Iqbal, 2014; Pegram and Jackisch, 2023; Sohrab, 2022). HER2 is a protein that plays a role in regulating cell growth and division (Iqbal and Iqbal, 2014). In some breast cancers, there is an overexpression or amplification of the HER2 gene, leading to an increased production of the HER2 protein (Iqbal and Iqbal, 2014). HER2- positive breast cancer is an important target in breast cancer treatment because the overexpression of HER2 is associated with more aggressive tumor growth and a poorer prognosis. Targeting HER2 can help slow down the progression of the cancer and improve treatment outcomes. In molecular docking studies, the HER2 (human epidermal growth factor receptor 2) protein is commonly used as a target protein, especially when investigating the binding of potential drug compounds or ligands (Sohrab, 2022). These therapies aim to be more effective and cause fewer side effects compared to traditional chemotherapy. Local Nigerian floras, also known as plants or plant species, have been studied for their potential roles in traditional medicine and complementary treatments, including the treatment of breast cancer. Some of these plants are believed to contain bioactive compounds with medicinal properties that could contribute to breast cancer treatment. However, it is important to note that while traditional remedies and plant-based compounds may show promise, they often need rigorous scientific validation before being recommended as standard treatments. Nigerian plant species that have been investigated for their potential roles in breast cancer treatment include; Annona muricata (Soursop or Graviola), Carica papaya (Papaya), Curcuma longa (Turmeric), Allium sativum (Garlic) and Azadirachta indica (Neem) (Ohiagu et al., 2021). It's important to emphasize that while these plants show potential, further research is needed to better understand their mechanisms of action, optimal dosages, and potential interactions with conventional breast cancer treatments. Scientific validation through preclinical and clinical studies is crucial before any plant-based remedies can be recommended for breast cancer treatment. Other Nigerian medicinal plants with great pharmacological and ethnobotanical properties include; Bryophyllum pinnatum (BP), Cassia sieberiana (CS), Cassia (CT) Tora and Tamarindus Indica (TI) (Archer et al., 2019; Meena and Niranjan, 2010; Pawar et al., 2011; Sarwa et al., 2014; Sookying and Duangjai, n.d.) (Fig. 1). These plants demonstrated plausible properties such as phytochemical, ethnobotanical, pharmacological and biological properties (Archer et al., 2019; Faboro et al., 2016; Khan and Odokpe, 2020; Meena and Niranjan, 2010; Ms and Ali, 2018; Salami et al., 2013; Sarwa et al., 2014; Sookying and Duangjai, n.d.). This study utilizes the potentials of BP, CB, CT and TI in the inhibition study of one of the breast cancer target proteins, HER2 through Insilco studies.
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