news

Deep-sea sugar EPS3.9 sparks immune attack on tumours

Posted: 29 July 2025 | | No comments yet

Scientists have isolated a sugar molecule from deep-sea bacteria that triggers pyroptosis – a form of inflammatory cell death – to halt tumour growth – highlighting the potential of marine microbes in drug development.

Scientists have discovered a new sugar molecule from deep-sea bacteria that could lead to new cancer therapies. The molecule, called EPS3.9, is an exopolysaccharide – a long-chain sugar – produced by the bacterium Spongiibacter nanhainus CSC3.9. According to the study, published in The FASEB Journal, EPS3.9 promotes pyroptosis – an inflammatory form of programmed cell death – effectively killing tumour cells and suppressing tumour growth.

What is pyroptosis and why does it matter?

Pyroptosis is a type of cell death distinct from apoptosis- characterised by inflammation and the release of signalling molecules that activate the immune system. This inflammatory response can be beneficial in cancer therapy, as it not only eliminates cancer cells but also recruits the body’s defences to attack tumours.

EPS3.9’s ability to induce pyroptosis presents a promising strategy for treating cancers that are resistant to conventional treatments, as it combines direct tumour killing with immune system activation.

 

Reserve your FREE place

 


Reduce preclinical failures with smarter off-target profiling

24 September 2025 | 15:00PM BST | FREE Webinar

Join this webinar to hear from Dr Emilie Desfosses as she shares insights into how in vitro and in silico methods can support more informed, human-relevant safety decisions -especially as ethical and regulatory changes continue to reshape preclinical research.

What you’ll learn:

  • Approaches for prioritizing follow-up studies and refining risk mitigation strategies
  • How to interpret hit profiles from binding and functional assays
  • Strategies for identifying organ systems at risk based on target activity modulation
  • How to use visualization tools to assess safety margins and compare compound profiles

Register Now – It’s Free!

 

The science behind EPS3.9’s action

Researchers isolated EPS3.9 from the deep ocean and analysed its chemical makeup, identifying mannose and glucose as its primary sugar components. Laboratory experiments demonstrated that EPS3.9 directly targets five specific membrane phospholipids on human leukaemia cells. This interaction triggers pyroptotic cell death- causing the cancer cells to swell and rupture, releasing inflammatory molecules.

Beyond cell cultures, EPS3.9 was tested in mice with liver tumours. The treated animals exhibited significant tumour shrinkage compared to untreated controls. The compound also appeared  to stimulate the immune system, suggesting a dual mechanism of tumour suppression.

Implications for future cancer therapies

“Our work not only provides a theoretical basis for developing more carbohydrate-based drugs but also highlights the importance of exploring marine microbial resources,” said Dr Chaomin Sun of the Chinese Academy of Sciences, corresponding author of the study.

The marine environment remains an underexplored reservoir of potentially powerful bioactive compounds. This study highlights how marine microbes can provide new molecules with unique mechanisms of action- such as EPS3.9’s ability to trigger pyroptosis.

Carbohydrate-based drugs are particularly appealing because sugars often exhibit low toxicity and high biocompatibility, making them promising candidates for drug development.

Challenges and next steps

While the findings are promising, EPS3.9 is still in the early stages of research. Scientists will need to investigate its safety profile, effectiveness across different cancer types and optimal delivery methods. Clinical trials will ultimately be required to determine whether EPS3.9 or related compounds can be developed into safe and effective cancer treatments for humans.

By harnessing nature’s biochemical diversity, researchers may be able to develop more effective, targeted treatments that both kill tumours and engage the immune system – potentially improving outcomes for cancer patients.