Due to rising incidence rates of liver cancer and worries about the toxicity of current chemotherapeutic medicines, the hunt for further alternative methods to treat this malignancy has escalated. Compared to chemotherapy, quercetin, a flavonoid, is relatively less harmful to normal cells and is regarded as an excellent free-radical scavenger. Apoptotic cell death of cancer cells caused by quercetin has been demonstrated by many prior studies. It is present in many fruits, vegetables, and herbs. Quercetin targets apoptosis, by upregulating Bax, caspase-3, and p21 while downregulating Akt, PLK-1, cyclin-B1, cyclin-A, CDC-2, CDK-2, and Bcl-2. Additionally, it has been reported to increase STAT3 protein degradation in liver cancer cells while decreasing STAT3 activation. Quercetin has a potential future in chemoprevention, based on substantial research on its anticancer effects. The current review discusses quercetin’s mechanisms of action, nanodelivery strategies, and other potential cellular effects in liver cancer.

Despite the immense therapeutic advances in the field of health sciences, cancer is still to be found among the global leading causes of morbidity and mortality. Ethnomedicinally, natural bioactive compounds isolated from various plant sources have been used for the treatment of several cancer types and have gained notable attention. Ferulic acid, a natural compound derived from various seeds, nuts, leaves, and fruits, exhibits a variety of pharmacological effects in cancer, including its proapoptotic, cell-cycle-arresting, anti-metastatic, and anti-inflammatory activities. This review study presents a thorough overview of the molecular targets and cellular signaling pathways modulated by ferulic acid in diverse malignancies, showing high potential for this phenolic acid to be developed as a candidate agent for novel anticancer therapeutics. In addition, current investigations to develop promising synergistic formulations are also discussed.

Carbon-based nanomaterials are contemporary and are outpacing the technology platform. Graphene quantum dots (GQDs) had a significant impact on the subject of bioengineering, pharmaceuticals, biomedicine, biosensors, fuel, energy, etc. Depending on how quickly this field is developing, it is important to recognize the new difficulties that GQDs have to overcome. This is incredibly significant because many novel applications and innovations that have made GQD synthesis easier recently have not been systematically evaluated in prior studies. Their ability to combine the benefits of quantum dots, sp² carbon materials (large specific surface area), and have rich functional groups at the edge makes them special. The naturally occurring inert carbon helps to stabilize chemical and physical characteristics and makes significant advancements in the creation of benchmark photocatalysts. Moreover, current challenges and potential of these rapidly developing GQDs are emphasized. The future of GQD research is limitless, according to the assessment in this review, notably if future research focuses on simplicity of purification and ecofriendly synthesis. This feature article offers a realistic summary on recent developments in the synthesis, characteristics, and uses of GQDs. Frequent review articles focusing on the progress of GQDs for specific applications are published but a thorough review article on GQDs for their numerous uses has not yet been published. The recent trends of scientific research based on new optical biosensing applications, including the comprehensive applications of different zero-dimensional nanomaterials, specially GQDs are discussed in this study.

For Drosophila melanogaster, cuticular melanisation is a quantitative trait, varying from no melanin to completely dark. Variation in melanisation has been linked with stress resistance, especially desiccation, in D. melanogaster and other species. As melanism has a genetic component, we selected melanic and non-melanic phenotypes of D. melanogaster in order to confirm the association of desiccation resistance and rate of water loss with cuticular melanisation previously reported for this species. A bidirectional selection experiment for dark (D₁–D₄) and light (L₁–L₄) body colour in D. melanogaster was conducted for 60 generations. We observed a 1.6-fold increase in abdominal melanisation in selected dark strains and a 14-fold decrease in selected light strains compared with control populations. Desiccation resistance increased significantly in the dark-selected morphs as compared with controls. The observed increase in desiccation resistance appeared as a consequence of a decrease in cuticular permeability. Our results show that traits related to water balance were significantly correlated with abdominal melanisation and were simultaneously selected bidirectionally along with melanisation.

Phloretin is a natural dihydrochalcone found in many fruits and vegetables, especially in apple tree leaves and the Manchurian apricots, exhibiting several therapeutic properties, such as antioxidant, antidiabetic, anti-inflammatory, and antitumor activities. In this review article, the diverse aspects of the anticancer potential of phloretin are addressed, presenting its antiproliferative, proapoptotic, antimetastatic, and antiangiogenic activities in many different preclinical cancer models. The fact that phloretin is a planar lipophilic polyphenol and, thus, a membrane-disrupting Pan-Assay Interference compound (PAIN) compromises the validity of the cell-based anticancer activities. Phloretin significantly reduces membrane dipole potential and, therefore, is expected to be able to activate a number of cellular signaling pathways in a non-specific way. In this way, the effects of this minor flavonoid on Bax and Bcl-2 proteins, caspases and MMPs, cytokines, and inflammatory enzymes are all analyzed in the current review. Moreover, besides the anticancer activities exerted by phloretin alone, its co-effects with conventional anticancer drugs are also under discussion. Therefore, this review presents a thorough overview of the preclinical anticancer potential of phloretin, allowing one to take the next steps in the development of novel drug candidates and move on to clinical trials.