Javascript must be enabled to continue!
ABCG2 Expression as a Potential Survival Predictor in Human Gliomas
View through CrossRef
Gliomas are notably challenging to treat due to their invasive nature and resistance to conventional therapies. The ABCG2 protein has attracted attention for its role in multidrug resistance, complicating treatment effectiveness. This study scrutinized the relationship between ABCG2 expression and glioma grade and the role of ABCG2 in the process of glioma progression, aiming to evaluate ABCG2 expression as a predictive factor of tumor progression and patient survival. Conducted at Dubrava University Hospital, Zagreb, Croatia, the study analyzed 152 glioma specimens from 2013 to 2022, assessing ABCG2 expression alongside standard clinical markers. A significant association was found between patients’ survival and the ABCG2 profile (p = 0.003, r = 0.24), separately for patients who underwent chemotherapy (p = 0.0004, r = 0.32) and radiotherapy (p = 0.003, r = 0.29). Furthermore, the ABCG2 profile was significantly associated with disease progression (p = 0.007, r = 0.23), tumor grade (p = 0.0002, r = 0.31), and Ki67 expression (p = 0.0004, r = 0.31). ABCG2-positive tumor cells only showed association with Ki67 expression (p = 0.002, r = 0.28). The ABCG2 profile was found to affect the overall patient survival (p = 0.02) and represent a moderate indicator of tumor progression (p = 0.01), unlike the percentage of ABCG2-positive tumor cells. ABCG2 may serve as a marker of angiogenesis and vascular abnormalities within tumors, predicting glioma progression and treatment response. Targeting ABCG2 could enhance chemoradiotherapy efficacy and improve patient outcomes, which highlights its value in assessing tumor aggressiveness and designing treatment strategies.
Title: ABCG2 Expression as a Potential Survival Predictor in Human Gliomas
Description:
Gliomas are notably challenging to treat due to their invasive nature and resistance to conventional therapies.
The ABCG2 protein has attracted attention for its role in multidrug resistance, complicating treatment effectiveness.
This study scrutinized the relationship between ABCG2 expression and glioma grade and the role of ABCG2 in the process of glioma progression, aiming to evaluate ABCG2 expression as a predictive factor of tumor progression and patient survival.
Conducted at Dubrava University Hospital, Zagreb, Croatia, the study analyzed 152 glioma specimens from 2013 to 2022, assessing ABCG2 expression alongside standard clinical markers.
A significant association was found between patients’ survival and the ABCG2 profile (p = 0.
003, r = 0.
24), separately for patients who underwent chemotherapy (p = 0.
0004, r = 0.
32) and radiotherapy (p = 0.
003, r = 0.
29).
Furthermore, the ABCG2 profile was significantly associated with disease progression (p = 0.
007, r = 0.
23), tumor grade (p = 0.
0002, r = 0.
31), and Ki67 expression (p = 0.
0004, r = 0.
31).
ABCG2-positive tumor cells only showed association with Ki67 expression (p = 0.
002, r = 0.
28).
The ABCG2 profile was found to affect the overall patient survival (p = 0.
02) and represent a moderate indicator of tumor progression (p = 0.
01), unlike the percentage of ABCG2-positive tumor cells.
ABCG2 may serve as a marker of angiogenesis and vascular abnormalities within tumors, predicting glioma progression and treatment response.
Targeting ABCG2 could enhance chemoradiotherapy efficacy and improve patient outcomes, which highlights its value in assessing tumor aggressiveness and designing treatment strategies.
Related Results
ABCG2 predicts the prognosis and is associated with immune infiltration in lung cancer: a bioinformatics study
ABCG2 predicts the prognosis and is associated with immune infiltration in lung cancer: a bioinformatics study
Abstract
Background
ATP-binding cassette superfamily G member 2 (ABCG2), a member of the ATP-binding cassette transporter family, is localized in the membrane of various h...
ABCG2 deficiency in skin impairs re‐epithelialization in cutaneous wound healing
ABCG2 deficiency in skin impairs re‐epithelialization in cutaneous wound healing
AbstractThe ATP‐binding cassette transporter ABCG2 is expressed in the interfollicular epidermis and mediates the side‐population phenotype in skin cells. However, the role of ABCG...
Abstract 1967: A-803467, a sodium channel blocker, reverses ABCG2-mediated MDR
Abstract 1967: A-803467, a sodium channel blocker, reverses ABCG2-mediated MDR
Abstract
The ATP-binding cassette, subfamily G, isoform 2 protein (ABCG2) is a vital member of the ABC transporter superfamily, which has been involved in multidrug ...
Constitutive Expression of the ATP-Binding Cassette Transporter ABCG2 Enhances the Growth Potential of Early Human Hematopoietic Progenitors
Constitutive Expression of the ATP-Binding Cassette Transporter ABCG2 Enhances the Growth Potential of Early Human Hematopoietic Progenitors
Abstract
The ATP-binding cassette transporter, ABCG2, is a molecular determinant of the side population phenotype, which is enriched for stem and progenitor cells in...
Abstract 1523: Caffeine antagonizes multidrug resistance by down-regulating ABCG2
Abstract 1523: Caffeine antagonizes multidrug resistance by down-regulating ABCG2
Abstract
ABCG2/BCRP (Breast Cancer Resistance Protein) is an ATP-binding-cassette (ABC) transporter that has been shown to confer multidrug resistance (MDR) in cance...
Interaction of Alcohol Consumption and ABCG2 rs2231142 Variant Contributes to Hyperuricemia in a Taiwanese Population
Interaction of Alcohol Consumption and ABCG2 rs2231142 Variant Contributes to Hyperuricemia in a Taiwanese Population
Background: ABCG2 rs2231142 is an important genetic factor that contributes to the development of gout and hyperuricemia (HUA). Epidemiologic studies have demonstrated that lifesty...
Abstract 4229: ATP-binding cassette transporter ABCG2/BCRP inhibition sensitizes CD133+ cells to MEK/BRAF inhibitors
Abstract 4229: ATP-binding cassette transporter ABCG2/BCRP inhibition sensitizes CD133+ cells to MEK/BRAF inhibitors
Abstract
Melanoma is a highly aggressive type of skin cancer. Melanoma-initiating cells (MIC) have self-renewal capacity, are highly tumorigenic and have been identi...
Sitravatinib Sensitizes ABCB1- and ABCG2-Overexpressing Multidrug-Resistant Cancer Cells to Chemotherapeutic Drugs
Sitravatinib Sensitizes ABCB1- and ABCG2-Overexpressing Multidrug-Resistant Cancer Cells to Chemotherapeutic Drugs
The development of multidrug resistance (MDR) in cancer patients driven by the overexpression of ATP-binding cassette (ABC) transporter ABCB1 or ABCG2 in cancer cells presents one ...

