Target intelligence / Profile preview

Histidine rich carboxyl terminus 1 (HRCT1)

Target
HRCT1
Molecular classification
Other (Structural protein; not classified as receptor, enzyme, transporter, etc.)
01

Overview

Histidine rich carboxyl terminus 1 (HRCT1) is a protein-coding human gene believed to be involved in maintaining epithelial integrity, possibly as a membrane or structural protein, especially in the alveolar epithelium. It is highly expressed in several tissues and displays altered transcript levels in certain malignancy states, including colorectal and liver cancer stem-like cells. There is insufficient evidence that HRCT1 functions as a receptor, enzyme, or any classical drug target, nor is it associated with recognized drug mechanisms or safety concerns. Instead, HRCT1’s role appears limited to basic cell and tissue structure. There is confusion involving histidine-rich proteins; for example, "histidine-rich calcium binding protein" is a completely different and well-characterized protein mostly in muscle tissue, and "histidine-rich glycoprotein" (HRG) is yet another distinct protein. No established drug targeting or molecular pathway is described for HRCT1, although its expression is altered in various cancers according to transcriptomic studies. In summary: HRCT1 is not a recognized therapeutic target, receptor, enzyme, transporter, or member of any classical druggable protein families. It is primarily classified as a structural protein, with possible roles in tissue integrity and cancer-associated gene expression, but its molecular function and therapeutic significance remain speculative.

Other names
Histidine-rich carboxyl terminus protein 1HRCT1UNQ338/PRO537LGLL338PRO537UNQ338
02

Biological functions

Structural integrity of membrane and tissueMay contribute to barrier function in alveolar epithelium (hypothesized, not confirmed)
03

Disease associations

Cancer (altered expression in stem-like cells in colorectal and liver cancers)Possibly involved in malignant transformation and progression in precancerous and cancerous lesions (based on transcriptomics in human colorectal and liver tissue)

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