AI Article Synopsis

  • Tuberculosis (TB) is a big health problem around the world, and many cases go undiagnosed, making treatment harder.
  • Understanding how our body's metabolic (energy) pathways work is important for finding new ways to treat both TB and its connections to lung cancer.
  • This research highlights how TB can lead to lung cancer and suggests that focusing on these metabolic pathways might help improve how we control and treat both diseases in the future.

Article Abstract

Despite the fact that some cases of tuberculosis (TB) are undiagnosed and untreated, it remains a serious global public health issue. In the diagnosis, treatment, and control of latent and active TB, there may be a lack of effectiveness. An understanding of metabolic pathways can be fundamental to treat latent TB infection and active TB disease. Rather than targeting , the control strategies aim to strengthen host responses to infection and reduce chronic inflammation by effectively enhancing host resistance to infection. The pathogenesis and progression of TB are linked to several metabolites and metabolic pathways, and they are potential targets for host-directed therapies. Additionally, metabolic pathways can contribute to the progression of lung cancer in patients with latent or active TB. A comprehensive metabolic pathway analysis is conducted to highlight lung cancer development in latent and active TB. The current study aimed to emphasize the association between metabolic pathways of tumor development in patients with latent and active TB. Health control programs around the world are compromised by TB and lung cancer due to their special epidemiological and clinical characteristics. Therefore, presenting the importance of lung cancer progression through metabolic pathways occurring upon TB infection can open new doors to improving control of TB infection and active TB disease while stressing that further evaluations are required to uncover this correlation.

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http://dx.doi.org/10.1080/15257770.2024.2308522DOI Listing

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