VitD Cancer Research Results

VitD, Vitamin D: Click to Expand ⟱
Source:
Type:
Vitamin D expression is decreased in: Breast, CRC, Prostate, Lung, Melanoma, GBM, Pancreatic cancer. (Poor prognosis, with decreased overall survival).
Vitamin D expression is increased in RCC, Thyroid, Ovarian, Endometrial, Cervical cancers (***Better prognosis, with increased overall survival).

See VDR and CYP27B1.
CYP27B1 is the enzyme responsible for converting 25‐hydroxyvitamin D into its active form, 1,25‐dihydroxyvitamin D (calcitriol). As with VDR, CYP27B1 expression in tumors has been investigated for its potential prognostic significance in various cancers.
What Vitamin D Reflects in Cancer
Low 25(OH)D commonly indicates:
-Reduced host resilience (frailty, sarcopenia risk)
-Impaired immune regulation (innate and adaptive)
-Higher inflammatory tone
-Less favorable tumor microenvironment signaling

Vitamin D status therefore integrates nutrition, inflammation, and immune competence.

How Vitamin D Is Used Clinically
A) Prognosis (Primary Use)
-Low vitamin D associates with worse outcomes across several cancers (observational consistency).
-Deficiency correlates with advanced disease and higher mortality.

B) Treatment Tolerance & Supportive Care
-Adequate levels support bone health, muscle function, and may reduce treatment-related complications.
-Correction of deficiency is standard supportive care in many oncology settings.

C) Immune Context (Adjunct)
-VDR signaling modulates cytokine balance, dendritic cell function, and T-cell responses.
-Status helps interpret immune readiness, but is not an immunotherapy selector.

Vitamin D is a meaningful host-state biomarker in oncology. Low levels signal reduced physiological and immune reserve and are associated with poorer outcomes. While it does not guide tumor-specific therapy, maintaining adequate vitamin D is clinically relevant for prognosis, tolerance, and supportive care—making it an important component of the host biomarker layer.


Scientific Papers found: Click to Expand⟱
3518- Bor,    Boron Report
- Review, Var, NA - Review, AD, NA
Risk↓, Boron reduces prostate cancer incidence by up to 64%
serineP↓, Boric acid acts to inhibit serine proteases—it decreases PSA by 87% and reduces tumor size in a prostate cancer mouse model
PSA↓,
TumVol↓,
IGF-1↓, expression of IGF-1 (insulin-like growth factor type 1) was markedly reduced by boron treatment. Circulating blood levels of IGF-1 were not reduced in the treated mice, however.
*Mag↑, In situations of adequate calcium supply but deficient magnesium resources, boron appears to substitute or “pinch hit” for magnesium during the process of bone formation.
*Calcium↑, The effect of boron on raising plasma calcium levels may, in part, be due to its enhancing effect on vitamin D.1
*VitD↑,
*COX2↓, boron has been shown to inhibit cyclooxygenase (COX) and lipoxygenase (LOX).
*5LO↓,
*PGE2↓, leads to a decrease in prostaglandin E2 (PGE2)
*NF-kB↓, suppressing nuclear factor kappa beta (NfkappaB)
*cognitive↑, Since it is now commonly accepted that the routine use of NSAIDs significantly reduces the incidence of Alzheimer’s disease,31,32 it is not surprising that papers have been published on boron’s positive effect on cognitive function.

3502- Bor,    Plasma boron concentrations in the general population: a cross-sectional analysis of cardio-metabolic and dietary correlates
- Review, NA, NA
*Half-Life↑, half-life of circulating boron after dietary intake is about 21 h [7]
*VitD↑, hypothesized that boron supplementation increases the biological half-live and bioavailability of vitamin D [4].
*cardioP↑, cardio-metabolic correlates of plasma boron concentrations, these cardio-protective benefits might be (at least partially) mediated by boron.
*RenoP↓, higher concentrations of boron within the body in individuals with slightly reduced kidney function, than pointing towards a direct detrimental effect of boron on renal function.

696- Bor,    Nothing Boring About Boron
- Review, Var, NA
*hs-CRP↓, reduces levels of inflammatory biomarkers, such as high-sensitivity C-reactive protein (hs-CRP) and tumor necrosis factor μ (TNF-μ);
*TNF-α↓,
*SOD↑, raises levels of antioxidant enzymes, such as superoxide dismutase (SOD), catalase, and glutathione peroxidase
*Catalase↑,
*GPx↑,
*cognitive↑, improves the brains electrical activity, cognitive performance, and short-term memory for elders; restricted boron intake adversely affected brain function and cognitive performance.
*memory↑, In humans, boron deprivation (<0.3 mg/d) resulted in poorer performance on tasks of motor speed and dexterity, attention, and short-term memory.
*Risk↓, Boron-rich diets and regions where the soil and water are rich in boron correlate with lower risks of several types of cancer, including prostate, breast, cervical, and lung cancers.
*SAM-e↑,
*NAD↝, Boron strongly binds oxidized NAD+,76 and, thus, might influence reactions in which NAD+ is involved
*ATP↝,
*Ca+2↝, Because of its positive charge, magnesium stabilizes cell membranes, balances the actions of calcium, and functions as a signal transducer
HDAC↓, some boronated compounds are histone deacetylase inhibitors
TumVol↓,
IGF-1↓, expression of IGF-1 in the tumors was significantly reduced by boron treatment
PSA↓, Boronic acid has been shown to inhibit PSA activity.
Cyc↓, boric acid inhibits the growth of prostate-cancer cells both by decreasing expression of A-E cyclin
TumCMig↓,
*serineP↓, Boron exists in the human body mostly in the form of boric acid, a serine protease inhibitor.
HIF-1↓, shown to greatly inhibit hypoxia-inducible factor (HIF) 1
*ChemoSideEff↓, An in vitro study found that boric acid can help protect against genotoxicity and cytotoxicity that are induced in lymphocytes by paclitaxel
*VitD↑, greater production of 25-hydroxylase, and, thus, greater potential for vitamin-D activation
*Mag↑, Boron significantly improves magnesium absorption and deposition in bone
*eff↑, boron increases the biological half-life and bioavailability of E2 and vitamin D.
Risk↓, risk of prostate cancer was 52% lower in men whose diets supplied more than 1.8 mg/d of boron compared with those whose dietary boron intake was less than or equal to 0.9 mg/d.
*Inflam↓, As research into the chemistry of boron-containing compounds has increased, they have been shown to be potent antiosteoporotic, anti-inflammatory, and antineoplastic agents
*neuroP↑, In addition, boron has anti-inflammatory effects that can help alleviate arthritis and improve brain function and has demonstrated such significant anticancer
*Calcium↑, increase serum levels of estradiol and calcium absorption in peri- and postmenopausal women.
*BMD↑, boron stimulates bone growth in vitamin-D deficient animals and alleviates dysfunctions in mineral metabolism characteristic of vitamin-D deficiency
*chemoP↑, may help ameliorate the adverse effects of traditional chemotherapeutic agents. boric acid can help protect against genotoxicity and cytotoxicity that are induced in lymphocytes by paclitaxel, an anticancer drug commonly used to treat breast, ovarian
AntiCan↑, demonstrated preventive and therapeutic effects in a number of cancers, such as prostate, cervical, and lung cancers, and multiple and non-Hodgkin’s lymphoma
*Dose↑, only an upper intake level (UL) of 20 mg/d for individuals aged ≥ 18 y.
*Dose↝, substantial number of articles showing benefits support the consideration of boron supplementation of 3 mg/d for any individual who is consuming a diet lacking in fruits and vegetables
*BMPs↑, Boron was also found to increase mRNA expression of alkaline phosphatase and bone morphogenetic proteins (BMPs)
*testos↑, 1 week of boron supplementation of 6 mg/d, a further study by Naghii et al20 of healthy males (n = 8) found (1) a significant increase in free testosterone,
angioG↓, Inhibition of tumor-induced angiogenesis prevents growth of many types of solid tumors and provides a novel approach for cancer treatment; thus, HIF-1 is a target of antineoplastic therapy.
Apoptosis↑, Cancer cells, however, commonly overexpress sugar transporters and/or underexpress borate export, rendering sugar-borate esters as promising chemopreventive agents
*selectivity↑, In normal cells, the 2 latter, cell-destructive effects do not occur because the amount of borate present in a healthy diet, 1 to 10 mg/d, is easily exported from normal cells.
*chemoPv↑, promising chemopreventive agents

758- Bor,    Comparative effects of daily and weekly boron supplementation on plasma steroid hormones and proinflammatory cytokines
- Human, NA, NA
*hs-CRP↓, Six hours supplementation showed a significant decrease on sex hormone binding globulin (SHBG), high sensitive CRP (hsCRP) and TNF-α level.
*TNF-α↓,
*SHBG↓,
*DHT↑, Dihydrotestosterone, cortisol and vitamin D was elevated.
*cortisol↑,
*VitD↑,
*BioAv↑, 11.6 mg of boron resulted in a significant increase in plasma boron concentration. Given such a fast bioavailabilit
*Inflam↓, Also, concentrations of all three inflammatory biomarkers decreased after supplementation.

759- Bor,    The nutritional and metabolic effects of boron in humans and animals
- in-vivo, NA, NA
DHT↑, testosterone
VitD↑,
HDL↓,

786- Mg,  VitC,    A narrative review on the role of magnesium in immune regulation, inflammation, infectious diseases, and cancer
Risk↓, boasts a significant anti-cancer effect.
*VitD↑, Mg is also essential for the synthesis and distribution of vitamin D
*pH↝, Additionally, the presence of Mg2+ plays a crucial role in regulating the levels of "intracellular free Ca2+ and intracellular pH"
*ROS↓, mitochondrial ROS inhibition (study in frail elderly patients)
TumCG↓, Mg in the diet slowed tumor development in young male rats
eff↑, Mg can enhance the anti-cancer effects of AA. (related to SVCT2 expression)

787- Mg,    Magnesium and Human Health: Perspectives and Research Directions
VitD↑, Mg is required for metabolism of vitamin D in the liver and the kidneys and also for its transportation in serum.
other↓, Lower stroke risk: Low magnesium intake is associated with an increased risk of stroke


Showing Research Papers: 1 to 7 of 7

* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 7

Pathway results for Effect on Cancer / Diseased Cells:


Redox & Oxidative Stress

HDL↓, 1,  

Cell Death

Apoptosis↑, 1,  

Transcription & Epigenetics

other↓, 1,  

Cell Cycle & Senescence

Cyc↓, 1,  

Proliferation, Differentiation & Cell State

HDAC↓, 1,   IGF-1↓, 2,   TumCG↓, 1,  

Migration

serineP↓, 1,   TumCMig↓, 1,  

Angiogenesis & Vasculature

angioG↓, 1,   HIF-1↓, 1,  

Immune & Inflammatory Signaling

PSA↓, 2,   VitD↑, 2,  

Hormonal & Nuclear Receptors

DHT↑, 1,  

Drug Metabolism & Resistance

eff↑, 1,  

Clinical Biomarkers

PSA↓, 2,   VitD↑, 2,  

Functional Outcomes

AntiCan↑, 1,   Risk↓, 3,   TumVol↓, 2,  
Total Targets: 20

Pathway results for Effect on Normal Cells:


Redox & Oxidative Stress

Catalase↑, 1,   GPx↑, 1,   ROS↓, 1,   SAM-e↑, 1,   SOD↑, 1,  

Mitochondria & Bioenergetics

ATP↝, 1,  

Core Metabolism/Glycolysis

NAD↝, 1,  

Migration

5LO↓, 1,   Ca+2↝, 1,   serineP↓, 1,  

Immune & Inflammatory Signaling

COX2↓, 1,   Inflam↓, 2,   NF-kB↓, 1,   PGE2↓, 1,   TNF-α↓, 2,   VitD↑, 5,  

Cellular Microenvironment

pH↝, 1,  

Hormonal & Nuclear Receptors

cortisol↑, 1,   DHT↑, 1,   SHBG↓, 1,   testos↑, 1,  

Drug Metabolism & Resistance

BioAv↑, 1,   Dose↑, 1,   Dose↝, 1,   eff↑, 1,   Half-Life↑, 1,   selectivity↑, 1,  

Clinical Biomarkers

BMD↑, 1,   BMPs↑, 1,   Calcium↑, 2,   hs-CRP↓, 2,   Mag↑, 2,   VitD↑, 5,  

Functional Outcomes

cardioP↑, 1,   chemoP↑, 1,   chemoPv↑, 1,   ChemoSideEff↓, 1,   cognitive↑, 2,   memory↑, 1,   neuroP↑, 1,   RenoP↓, 1,   Risk↓, 1,  
Total Targets: 42

Scientific Paper Hit Count for: VitD, Vitamin D
5 Boron
2 Magnesium
1 Vitamin C (Ascorbic Acid)
Query results interpretion may depend on "conditions" listed in the research papers.
Such Conditions may include : 
  -low or high Dose
  -format for product, such as nano of lipid formations
  -different cell line effects
  -synergies with other products 
  -if effect was for normal or cancerous cells
Filter Conditions: Pro/AntiFlg:%  IllCat:%  CanType:%  Cells:%  prod#:%  Target#:851  State#:%  Dir#:2
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