Marine herbal medicine generally refers to the use of marine plants as original materials to develop crude drugs, or for other medical purposes. The term 'marine plants' usually denotes macroalgae grown between intertidal and subintertidal zones, including Chlorophyta, Phaeophyta, and Rhodophyta. Considerable progress has been made in the field of biomedical research into marine microalgae and microorganisms in the past decade. As the most important source of fundamental products in the world, marine plants have a very important role in biomedical research.Furthermore, worldwide studies have consistently demonstrated that many crude drugs derived from marine plants contain novel ingredients that may benefit health or can be used in the treatment of diseases; some have been developed into health foods, and some even into drugs. It is expected that there are many substances of marine plant origin that will have medical applications in terms of improving human health and are awaiting discovery.With the opening of this Special Issue, we aim to draw attention to the scientific research and potential utilization of marine herbal medicines.Abstract: Chemotherapy drugs for oral cancers always cause side effects and adverse effects. Currently natural sources and herbs are being searched for treated human oral squamous carcinoma cells (OSCC) in an effort to alleviate the causations of agents in oral cancers chemotherapy. This study investigates the effect of prodigiosin (PG), an alkaloid and natural red pigment as a secondary metabolite of Serratia marcescens, to inhibit human oral squamous carcinoma cell growth; thereby, developing a new drug for the treatment of oral cancer. In vitro cultured human OSCC models (OECM1 and SAS cell lines) were used to test the inhibitory growth of PG via cell cytotoxic effects (MTT assay), cell cycle analysis, and Western blotting. PG under various concentrations and time courses were shown to effectively cause cell death and cell-cycle arrest in OECM1 and SAS cells. Additionally, PG induced autophagic cell death in OECM1 and SAS cells by LC3-mediated P62/LC3-I/LC3-II pathway at the in vitro level. These findings elucidate the role of PG, which may target the autophagic cell death pathways as a potential agent in cancer therapeutics.Autophagy has been shown to be an intracellular degradation process in eukaryotic cells in response to stress, including starvation, clearing damaged proteins and organelles, and promoting cell survival [4,5]. Furthermore, autophagy occurs in multiple processes including nucleation, expansion, and maturation/retrieval to exert the effects of either autophagic cell death or cytoprotection [6]. Currently, two pathways have been investigated to associate with the regulation of autophagy in mammalian cells including the PI3K Class III/Akt/mTOR/p70S6K signaling pathway and the Ras/Raf/MEK/ERK1/2 pathway [7,8]. The ERK1/2 pathway could positively activate autophagy, whereas the Akt/mTOR pathway might suppress autophagy. These signaling pathways could be activated in ...