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Study breakdown

Both Ghrelin AND Des-Acyl Ghrelin Stimulate Adrenal Cancer Cell Growth

In VitroPreliminary evidence
The takeaway

Both acylated ghrelin and des-acyl ghrelin stimulated adrenocortical tumor cell proliferation through anti-apoptotic pathways, confirming the ghrelin system promotes growth in at least some cancer types regardless of acylation status.

Key finding

Both ghrelin and des-acyl ghrelin stimulated adrenocortical tumor cell proliferation via anti-apoptotic pathway activation (reduced caspase-3, increas

What the researchers found

Both ghrelin and des-acyl ghrelin stimulated adrenocortical tumor cell proliferation via anti-apoptotic pathway activation (reduced caspase-3, increased Bcl-2), demonstrating pro-tumorigenic ghrelin system activity in adrenal cancer regardless of GHS-R1a-dependent signaling.

Why it matters

Relevant for ghrp, cancer, hormone-optimization.

How the study worked

in-vitro study on ghrp, cancer.

What this study cannot tell us

See abstract.

How to read the evidence

preliminary evidence.

When this study was published

Published in 2007.

The bigger picture

Advances peptide research.

Questions still open

  • Further research needed.
  • Clinical translation to evaluate.

Common questions

What was studied?
Both Ghrelin AND Des-Acyl Ghrelin Stimulate Adrenal Cancer Cell Growth
What was found?
Both acylated ghrelin and des-acyl ghrelin stimulated adrenocortical tumor cell proliferation through anti-apoptotic pathways, confirming the ghrelin system promotes growth in at least some cancer types regardless of acylation status.

Read the original research

Ghrelin and its unacylated isoform stimulate the growth of adrenocortical tumor cells via an anti-apoptotic pathway.

American journal of physiology. Endocrinology and metabolism, 293(1), E302-9

Citation

Delhanty, P J D; van Koetsveld, P M; Gauna, C; van de Zande, B; Vitale, G; Hofland, L J; van der Lely, A J. (2007). Ghrelin and its unacylated isoform stimulate the growth of adrenocortical tumor cells via an anti-apoptotic pathway.. American journal of physiology. Endocrinology and metabolism, 293(1), E302-9.