Shabnum S Sameera, Siranjeevi R, Raj C Krishna, Saravanan A, Vickram A S, Chopra Hitesh, Malik Tabarak
Department of Chemistry, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences, Saveetha University Chennai-602105 Tamil Nadu India
Department of Sustainable Engineering, Institute of Biotechnology, Saveetha School of Engineering, SIMATS Chennai-602105 Tamil Nadu India.
RSC Adv. 2024 Dec 10;14(52):38952-38995. doi: 10.1039/d4ra07114j. eCollection 2024 Dec 3.
Cancer is a disease that involves uncontrolled cell division triggered by genetic damage to the genes that control cell growth and division. Cancer starts as a localized illness, but subsequently spreads to other areas in the human body (metastasis), making it incurable. Cancer is the second most prevalent cause of mortality worldwide. Every year, almost ten million individuals get diagnosed with cancer. Although different cancer treatment options exist, such as chemotherapy, radiation, surgery and immunotherapy, their clinical efficacy is limited due to their significant side effects. New cancer treatment options, such as phototherapy, which employs light for the treatment of cancer, have sparked a growing fascination in the cancer research community. Phototherapies are classified into two types: photodynamic treatment (PDT) and photothermal therapy (PTT). PDT necessitates the use of a photosensitizing chemical and exposure to light at a certain wavelength. Photodynamic treatment (PDT) is primarily based on the creation of singlet oxygen by the stimulation of a photosensitizer, which is then used to kill tumor cells. PDT can be used to treat a variety of malignancies. On the other hand, PTT employs a photothermal molecule that activates and destroys cancer cells at the longer wavelengths of light, making it less energetic and hence less hazardous to other cells and tissues. While PTT is a better alternative to standard cancer therapy, in some irradiation circumstances, it can cause cellular necrosis, which results in pro-inflammatory reactions that can be harmful to therapeutic effectiveness. Latest research has revealed that PTT may be adjusted to produce apoptosis instead of necrosis, which is attractive since apoptosis reduces the inflammatory response.
癌症是一种由控制细胞生长和分裂的基因发生遗传损伤引发的、涉及细胞不受控制地分裂的疾病。癌症起初是一种局部性疾病,但随后会扩散到人体的其他部位(转移),从而变得无法治愈。癌症是全球第二大常见死因。每年,近一千万人被诊断出患有癌症。尽管存在不同的癌症治疗选择,如化疗、放疗、手术和免疫疗法,但由于其显著的副作用,它们的临床疗效有限。新的癌症治疗选择,如利用光来治疗癌症的光疗法,在癌症研究界引发了越来越浓厚的兴趣。光疗法分为两种类型:光动力疗法(PDT)和光热疗法(PTT)。光动力疗法需要使用一种光敏化学物质并暴露于特定波长的光下。光动力疗法(PDT)主要基于通过刺激光敏剂产生单线态氧,然后利用单线态氧杀死肿瘤细胞。光动力疗法可用于治疗多种恶性肿瘤。另一方面,光热疗法使用一种光热分子,该分子在较长波长的光下激活并破坏癌细胞,使其能量较低,因此对其他细胞和组织的危害较小。虽然光热疗法是标准癌症治疗的更好替代方法,但在某些照射情况下,它会导致细胞坏死,从而引发促炎反应,这可能对治疗效果有害。最新研究表明,光热疗法可以进行调整以产生凋亡而非坏死,这很有吸引力,因为凋亡会减少炎症反应。