Прогастрин

Прогастрин представляет собой 80- аминокислотный внутриклеточный белок и предшественник гастрина , желудочно-кишечного гормона, продуцируемого G-клетками в желудочном антруме. Основной функцией гастрина является регулирование кислотной секреции. Во время пищеварения только гастрин выделяется в кровоток и стимулирует секрецию соляной кислоты в желудке, а также поджелудочной железы пищеварительные ферменты . У людей прогастрин кодируется гастом ген. Прогастрин экспрессируется в основном в ткани желудка .

Открытие

В 1905 году Джон Сидни Эдкинс продемонстрировал существование гормона, ответственного за секрецию желудочной кислоты. Этот гормон был назван желудочным секретаном или гастрином . только в 1979 году и позднее в 1987 и 1988 годах прогноз был идентифицирован как предшественник гастрина Но . Его белковая последовательность и мРНК были выявлены.

Не путать с прогастрином, релизирующий пептид , предшественник релизирующего гастрина (GRP), нейропептида , который принадлежит к семейству бомбесина /нейромедина B и чья экспрессия важна в кишечнике и мозге . GRP участвует во многих физиологических и патофизиологических процессах. Отмещающий гастрин пептид стимулирует высвобождение гастрина и других желудочно-кишечных гормонов . Это помогает регулировать потребление пищи . Существует также два типа прогастрина, внутриклеточный прогастрин, обсуждаемый в этой статье и внеклеточный прогастрин, в основном называемый HPG80 .

Structure and production

The GAST gene is located on chromosome 17 (17q21). It consists of three exons containing the sequence that encodes preprogastrin. Progastrin is made up of several alpha helices. The primary structure of human preprogastrin consists of a 21 amino acid signal sequence at the N-terminus followed by a spacer peptide, a bioactive domain and finally a C-terminal flanking peptide (CTFP).

Action

The production of gastrin allows the production of gastric acid during food intake to be promoted. Progastrin has also been shown to be expressed in other healthy tissues (cerebellum, pituitary gland, pancreas, testicles), but to a much lesser extent than in the stomach and in different forms. For example, carboxyamide gastrin is found in the testicles. However, the role of progastrin in these organs is not clearly established.

Biosynthesis

In humans, the GAST gene encodes a 101-amino acid precursor peptide, preprogastrin. The latter is synthesized and matured in the endoplasmic reticulum. Upon initiation of translation, the signal sequence facilitating the translocation of the polypeptide is eliminated by a membrane-bound signal peptidase. This enzyme cleaves the born polypeptide chain between alanine residue 21 and serine 22 to generate the 80-amino acid peptide progastrin. The progastrin is then cleaved by an enzyme to give the main circulating biologically active forms of gastrin: gastrin-34 and gastrin-17, in sulfated and unsulfated forms. Both sulfation and phosphorylation play a role in the maturation process: they increase the maturation of progastrin. While phosphorylation can also affect the conversion of intermediate products with carboxy-terminal glycine (G34-Gly and G17-Gly) to mature gastrins. Small amounts of gastrin-52 (also called component 1), gastrin-14 (mini-gastrin) and even smaller fragments were detected in the serum. At this stage, two pathways of post-translational modifications exist within the antral G cells. In the dominant pathway, progastrin is cleaved at three sites, resulting in two major bioactive gastrins, gastrin-34 and gastrin-17. In the putative alternative pathway, progastrin can be cleaved only at the dibasic site closest to the C-terminus, resulting in the synthesis of gastrin-71. The other maturation products, in particular G34-Gly, G17-Gly and CTFP have various functions. CTFP has been described as capable of inducing or inhibiting apoptosis, depending on the tissue or cell type involved. After the progastrin conversion step, there is a passage through the secretory pathway.

Under pathological conditions

As early as 1996, it was demonstrated that the expression of the GAST gene is required for the cellular tumorigenicity of human colorectal cancer. The GAST gene has been shown to be a downstream target of the β-catenin/TCF-4 signalling pathway. Transfection of a construct expressing a constitutively active form of β-catenin triples the activity of the GAST gene promoter. This study establishes a link between progastrin and cancer across many cellular functions involving the Wnt pathway in a cancer cell, starting with its importance for cancer stem cell survival. In pathological situations, progastrin is secreted by tumor cells into the bloodstream and is referred to as hPG80.

The expression of progastrin in many cancers has been demonstrated. It has been noted that in colorectal cancers, progastrin is more than 700 times more abundant than amidated gastrin. Another study showed that colorectal carcinomas have progastrin-derived peptides that are not converted to gastrin. Finally, it has been shown that half of the tumor cells express progastrin. Ovarian, liver and pancreatic cancers present the same scenario: unmatured progastrin is more abundant than amidated gastrin. This is because progastrin is not fully matured and is secreted into the bloodstream for many cancers.