skin & beauty
RUNX3

The Involvement of a Complex Cellular Pathway in Male-Pattern Baldness (RUNX3)

Written by Shany Lahan, MS (Neuroscience) on December 28th, 2020
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RUNX3 may be involved in hair follicle cell death. How might variants of RUNX3 promote male-pattern baldness? Read more to find out.

Summary

RUNX3 codes for an essential component of the TGF-beta signaling pathway, which may promote cell death in hair follicles. Variants of RUNX3 may play a role in male-pattern baldness by increasing production of RUNX3 and potentiating TGF-beta pathway activity. Lifestyle, diet, and supplement modifications may counteract the effects of these variants by decreasing activity of the TGF-beta signaling pathway.

RUNX3 and Male-Pattern Baldness

The RUNX3 gene codes for RUNX family transcription factor 3 (RUNX3), a protein that alters gene activity [R]. 

RUNX3 has been shown to play an integral role in the TGF-beta signaling pathway. This pathway may contribute to a wide array of cellular processes, including cell growth, cell specialization, and cell death [R, R, R]. 

For example, the TGF-beta pathway may help regulate the hair growth cycle, in which hair grows within follicles, hair follicles regress, and hair falls out [R].

In cells of the hair follicle, heightened activity of the TGF-beta pathway has been suggested to prematurely initiate hair follicle regression and in turn, shorten the hair growth cycle [R].

Variants of RUNX3 have been associated with male-pattern baldness. These variants may increase RUNX3 activity, resulting in excessive cell death within hair follicles and consequent hair loss [R, R].

Your RUNX3 Results for Male-Pattern Baldness

SNP Table

variant genotype frequency risk allele
rs760805
rs742230
rs7517302

 

Primary SNP:

RUNX3 rs760805 [R]

  • ‘A’ = Higher odds of male-pattern baldness, relative to ‘T’
  • ‘T’ = Lower odds of male-pattern baldness, relative to ‘A’

Other Important SNPs:

RUNX3 rs742230 [R]

  • ‘G’ = Higher odds of male-pattern baldness, relative to ‘A’
  • ‘A’ = Lower odds of male-pattern baldness, relative to ‘G’

RUNX3 rs7517302 [R]

  • ‘C’ = Higher odds of male-pattern baldness, relative to ‘T’
  • ‘T’ = Lower odds of male-pattern baldness, relative to ‘C’

 

Recommendations

Lifestyle

Avoid Cigarettes

Cigarette smoke is well-known to stimulate the TGF-beta pathway, suggesting that it may worsen the effects of RUNX3 risk variants [R, R, R, R, R].

Several studies have associated smoking with an approximately 2-fold increased risk of male-pattern baldness. Cigarette smoke may cause oxidative and inflammatory damage in the hair follicles, impair hair growth, and reduce female sex hormone levels. A study found that the combination of smoking with being overweight increased male-pattern baldness severity [R, R, R, R, R].

Cigarettes may stimulate the TGF-beta pathway. Avoiding cigarettes may therefore help manage male-pattern baldness by preventing excessive TGF-beta signaling pathway stimulation.  

Diet

Mediterranean Diet

Olive oil is the main source of fat in the Mediterranean diet. Olive oil has been found to lower TGF-beta pathway activity in multiple studies [R, R].

In a study of men, the incidence of male-pattern baldness was reduced by over 50% in those consuming a Mediterranean diet rich in fresh vegetables (3 or more per week) and herbs (3 or more regularly) [R].

The Mediterranean diet may help manage male-pattern baldness by decreasing activity of the TGF-beta signaling pathway.

Supplements

Topical Caffeine

Caffeine has been suggested to promote the growth of hair by reducing TGF-beta signaling pathway activity [RR].

Topical lotions and shampoos with caffeine increased hair strength and thickness while decreasing hair loss in 4 trials of men with male-pattern baldness. The lotion enhanced the effectiveness of minoxidil (a conventional medication) in one of them [R, R, R, R].

Similarly, a shampoo with caffeine used for 6 months reduced hair loss and increased hair strength in women in one trial [R].

Caffeine may help manage male-pattern baldness by decreasing activity of the TGF-beta signaling pathway.

Author photo
Shany Lahan
MS (Neuroscience)

Shany received her MSc in Neuroscience from Western University.

Prior to joining SelfDecode, Shany conducted research related to Alzheimer’s disease, and taught science to undergraduate students. She believes that research should be accessible to everyone, regardless of scientific background. Shany joined SelfDecode with a mission to help others optimize their health and wellbeing – as well as help them understand the science behind it all.

Disclaimer

The information on this website has not been evaluated by the Food & Drug Administration or any other official medical body. This information is presented for educational purposes only, and may not be used to diagnose or treat any illness or disease.

Also keep in mind that the “Risk Score” presented in this post is based only on a select number of SNPs, and therefore only represents a small portion of your total risk as an individual. Furthermore, these analyses are based primarily on associational studies, which do not necessarily imply causation. Finally, many other (non-genetic) factors can also play a significant role in the development of a disease or health condition — therefore, carrying any of the risk-associated genotypes discussed in this post does not necessarily mean you are at increased risk of developing a major health condition.

Always consult your doctor before acting on any information or recommendations discussed in this post — especially if you are pregnant, nursing, taking medication, or have been officially diagnosed with a medical condition.

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