BMX

Case Study 1: Xiuxiu Li, 2023

Prostate cancer is highly dependent on androgens and the androgen receptor (AR). Hormonal therapies inhibit gonadal testosterone production, block extragonadal androgen biosynthesis, or directly antagonize AR. Resistance to medical castration occurs as castration-resistant prostate cancer (CRPC) and is driven by reactivation of the androgen-AR axis. 3β-hydroxysteroid dehydrogenase-1 (3βHSD1) serves as the rate-limiting step for potent androgen synthesis from extragonadal precursors, thereby stimulating CRPC. Genetic evidence in men demonstrates the role of 3βHSD1 in driving CRPC. In postmenopausal women, 3βHSD1 is required for synthesis of aromatase substrates and plays an essential role in breast cancer. Therefore, 3βHSD1 lies at a critical junction for the synthesis of androgens and estrogens, and this metabolic flux is regulated through germline-inherited mechanisms. This study shows that phosphorylation of tyrosine 344 (Y344) occurs and is required for 3βHSD1 cellular activity and generation of Δ4, 3-keto-substrates of 5α-reductase and aromatase, including in patient tissues. BMX directly interacts with 3βHSD1 and is necessary for enzyme phosphorylation and androgen biosynthesis. In vivo blockade of 3βHSD1 Y344 phosphorylation inhibits CRPC.

Fig1. 293T cells were transiently cotransfected with HA-BMX, EGFR, SRC, or YES and GST-3βHSD1, followed by GST pull-down and Western blot (left).

Fig2. Cells with cooverexpression of GST-3βHSD1 and HA-BMX or vehicle were treated with DHEA for 1 hour.

Case Study 2: Sen Chen, 2018

Prostate cancer responds to therapies that suppress androgen receptor (AR) activity (androgen deprivation therapy, ADT) but invariably progresses to castration-resistant prostate cancer (CRPC). The Tec family nonreceptor tyrosine kinase BMX is activated downstream of PI3K and has been implicated in regulation of multiple pathways and in the development of cancers including prostate cancer. However, its precise mechanisms of action, and particularly its endogenous substrates, remain to be established.

Here, the researchers demonstrate that BMX expression in prostate cancer is suppressed directly by AR via binding to the BMX gene and that BMX expression is subsequently rapidly increased in response to ADT. BMX contributed to CRPC development in cell line and xenograft models by positively regulating the activities of multiple receptor tyrosine kinases through phosphorylation of a phosphotyrosine-tyrosine (pYY) motif in their activation loop, generating pYpY that is required for full kinase activity. To assess BMX activity in vivo, they generated a BMX substrate-specific antibody (anti-pYpY) and found that its reactivity correlated with BMX expression in clinical samples, supporting pYY as an in vivo substrate. Inhibition of BMX with ibrutinib (developed as an inhibitor of the related Tec kinase BTK) or another BMX inhibitor BMX-IN-1 markedly enhanced the response to castration in a prostate cancer xenograft model.

Fig3. HEK 293 cells double transfected with wild type FAK and wild type or kinase dead BMX (or empty vector, EV) were treated with or without 1 μM ibrutinib for 4 hr.

Fig4. BMX Affymetrix expression prior to therapy (control), after 7 days of abiraterone (d7), or at relapse on abiraterone or after castration in LuCaP PDX models.

Fig1. Proposed model for 3βHSD1 phosphorylation. BMX phosphorylates 3βHSD1 Y344 upon activation by DHEA. (Xiuxiu Li, 2023)

Fig2. A schematic diagram of the BMX-mediated AKT and STAT3 pathway activation in human cervical cancer cells. (Yuanyuan Li, 2017)

BMX involved in several pathways and played different roles in them. We selected most pathways BMX participated on our site, such as Angiopoietin receptor Tie2-mediated signaling, Apoptosis, Apoptotic cleavage of cellular proteins, which may be useful for your reference. Also, other proteins which involved in the same pathway with BMX were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

BMX has several biochemical functions, for example, ATP binding, metal ion binding, non-membrane spanning protein tyrosine kinase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by BMX itself. We selected most functions BMX had, and list some proteins which have the same functions with BMX. You can find most of the proteins on our site.

BMX has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with BMX here. Most of them are supplied by our site. Hope this information will be useful for your research of BMX.

STAT3; PIM1; PIM1; saicar; EGFR; ERBB2; PKM; TP53; HSP90AB1; CRK; CLNK